Table 2.
RP11- clone | chromosome | F statistic | Adjusted p-values | Interaction p-values | Smoking main p-values | Gain/Loss/Either | Chromosome Region (bp) | candidate genes in region |
---|---|---|---|---|---|---|---|---|
422P24 | 1q21.3 | 7.806 | 0.060 | 0.400 | 0.373 | Either | 148,810,010–150,938,155 | S100 protein family |
| ||||||||
525G13 | 1q23.3 | 12.997 | 0.008 | 0.998 | 0.115 | Gain | 162,588,522–162,784,903 | UCK2 |
| ||||||||
544B14 | 1q32.1 | 13.209 | 0.007 | 0.105 | 0.199 | Gain/Either | 203,329,259–203,409,712 | IL10, IL19 |
| ||||||||
115P16 | 8.086 | 0.084 | 0.651 | 0.231 | ||||
520H14 | 1q42.1-q43 | 7.404 | 0.122 | 0.698 | 0.280 | Gain | 222,516,739–228,034,708 | RHOU, ADPRT, TSNAX, CAPN9, WNT3A, WNT9A |
12H2 | 8.086 | 0.084 | 0.651 | 0.231 | ||||
| ||||||||
375H24 | 1q42.13 | 7.608 | 0.109 | 0.619 | 0.253 | Gain/Either | 223,281,925–224,613,365 | WNT3A, WNT9A |
| ||||||||
334N15 | 2q24.3 | 8.741 | 0.059 | 0.450 | 0.757 | Gain | 167,814,597–169,454,975 | STK39 |
| ||||||||
204J18 | 3p14.2 | 7.920 | 0.091 | 0.124 | 0.404 | Gain | 60,927,060–62,456,006 | FHIT, PTPRG, ID2B |
| ||||||||
90K6 | 3q13.2 | 8.520 | 0.066 | 0.322 | 0.234 | Gain | 113,221,207–114,199,281 | CD200 |
| ||||||||
240H8 | 10.016 | 0.029 | 0.064 | 0.029 | ||||
160L16 | 10.016 | 0.029 | 0.064 | 0.029 | ||||
66O14 | 10.144 | 0.028 | 0.049 | 0.041 | ||||
627P22 | 10.016 | 0.029 | 0.064 | 0.029 | ||||
600K23 | 10.016 | 0.029 | 0.064 | 0.029 | ||||
54N19 | 10.016 | 0.029 | 0.064 | 0.029 | ||||
16G1 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
95N10 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
115G23 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
609L3 | 8.742 | 0.059 | 0.040 | 0.068 | ||||
138E20 | 8.398 | 0.071 | 0.043 | 0.064 | ||||
87M15 | 7p21.1–p11.2 | 9.033 | 0.051 | 0.040 | 0.060 | Gain/Either | 19,394,202–55,274,090 | EGFR, IL6, HUS1, INHBA, GLI3, VRAL, MYCLK1, IGFBP3 |
85E16 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
75O22 | 7.523 | 0.114 | 0.044 | 0.082 | ||||
121A8 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
462D19 | 8.457 | 0.069 | 0.133 | 0.050 | ||||
100C21 | 9.146 | 0.048 | 0.031 | 0.078 | ||||
111K18 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
137P13 | 9.146 | 0.048 | 0.031 | 0.078 | ||||
84O18 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
832D10 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
81B20 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
339F13 | 9.033 | 0.051 | 0.040 | 0.060 | ||||
97P11 | 7.167 | 0.138 | 0.071 | 0.030 | ||||
| ||||||||
251I15 | 7p11.2 | 10.772 | 0.011 | 0.036 | 0.047 | Either | 55,274,090–55,781,496 | |
| ||||||||
86P18 | 7.957 | 0.090 | 0.203 | 0.048 | ||||
92J13 | 7.957 | 0.090 | 0.203 | 0.048 | ||||
78C11 | 7q31.1-q31.32 | 7.957 | 0.090 | 0.203 | 0.048 | Gain | 106,955,503–121,128,048 | MET, WNT2, CYR61, ING3, DOCK4, CBLL1 |
110C11 | 7.957 | 0.090 | 0.203 | 0.048 | ||||
95L16 | 7.957 | 0.090 | 0.203 | 0.048 | ||||
140O21 | 7.957 | 0.090 | 0.203 | 0.048 | ||||
| ||||||||
247A12 | 8.307 | 0.049 | 0.660 | 0.129 | ||||
409K20 | 9q34.11-q34.13 | 8.307 | 0.049 | 0.660 | 0.129 | Loss | 128,543,247–130,681,562 | ABL1 |
618A20 | 8.307 | 0.049 | 0.660 | 0.129 | ||||
| ||||||||
173B14 | 7.316 | 0.082 | 0.440 | 0.006 | ||||
318G21 | 13q21.1-q31.3 | 7.316 | 0.082 | 0.440 | 0.006 | Either | 73,769,921–81,136,723 | MYCBP2 |
600P1 | 8.348 | 0.043 | 0.548 | 0.002 | ||||
| ||||||||
238I24 | 14q24.3-qter | 10.815 | 0.012 | 0.708 | 0.052 | Loss | 101,461,362–106,368,585 | XRCC3, MARK3, ASPP1, AKT1, HSPCA |
815P21 | 10.815 | 0.012 | 0.708 | 0.052 | ||||
| ||||||||
1057H19 | 11.557 | 0.008 | 0.376 | 0.085 | ||||
22M5 | 11.680 | 0.007 | 0.291 | 0.150 | ||||
297B9 | 11.680 | 0.007 | 0.291 | 0.150 | ||||
389H23 | 11.680 | 0.007 | 0.291 | 0.150 | ||||
540P6 | chr22 | 11.680 | 0.007 | 0.291 | 0.150 | Loss | CHK2, BCR, TOP3B, p300, NF2, ST13, TIMP3 | |
1078O11 | 13.257 | 0.003 | 0.266 | 0.063 | ||||
395B24 | 13.257 | 0.003 | 0.266 | 0.063 | ||||
1021O19 | 13.211 | 0.003 | 0.266 | 0.063 | ||||
1113I2 | 9.728 | 0.021 | 0.402 | 0.034 |
Gain = associated with genome-wide copy number amplification
Loss = associated with genome-wide copy number deletion
Either = associated with genome-wide copy number aberration
BACs correlated with overall genomic instability (estimated proportions of copy number aberrations) at an adjusted p-value <0.10. F-statistics correspond to the full model fit described in the methods section. The adjusted p-values are calculated with respect to the adjusted distribution (obtained via permutation) of the maximum F statistic. The p-values listed for smoking status by BAC interactions and smoking status main effects are marginal. Values significant at p<0.05 are in bold. The adjusted p-values are calculated with respect to the permutation distribution discussed in the methods section. Interaction and smoking main effect p-values correspond to the un-adjusted p-values associated with the f-tests for the comparison of the full model to reduced model 1 and the comparison of reduced model 1 to reduced model 2, respectively.