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. 2016 Oct 18;10(Suppl 7):103–108. doi: 10.1186/s12919-016-0013-1

Table 2.

Annotated transcript and SNP table

Transcript Gene Chromosome Start Length SNP DBSnp rs SNP annotation
GI_42544126-I SF1 chr11 64532075 14241 11_64511322 rs2073798 RASGRP2 intron
11_64519345 rs686171 PYGM intron
11_64546106 rs3741398 SF1 2 kb upstream, nc transcript variant, 5’ UTR
11_64546257 rs1633462 SF1 2 kb upstream, nc transcript variant, 5’ UTR
11_64573589 rs669976 MEN1 intron
11_64576598 rs67808744 MEN1 intron
11_64577620 rs7949944 MEN1 5’ UTR, 2 kb upstream
GI_23097237-S CHST13 chr3 126243130 19004 3_126218788 rs6774768 UROC1 intron
3_126228953 rs1873388 UROC1 intron
3_126242964 rs1388096 CHST13 2 kb upstream
3_126245956 rs4592980 CHST13 intron/3’UTR
3_126246370 rs1994642 CHST13 intron/3’UTR
3_126247795 rs11717719 CHST13 intron
3_126247848 rs11718493 CHST13 intron
GI_10863968-S POLD4 chr11 67119018 2034 11_67196237 rs1476792
Hs.283934-S TSPAN16 chr19 11406815 30857 19_11340057 rs17001244
19_11358700 rs4804579
19_11374675 rs416231
19_11380295 rs4804159
19_11406952 rs374409
GI_12056480-A UTS2 chr1 7907271 6280 1_7710810 rs58905635 CAMTA1 intron
1_7725855 rs4908471 CAMTA1 intron
1_7749807 rs3124797 CAMTA1 intron
GI_20986517-S MAPK8IP1 chr11 45907046 20970 11_45838926 rs11038668
11_45840939 rs7112505
11_45891418 rs7123390 CRY2 intron
Hs.58104-S FAM101B chr17 289771 8960 17_185027 rs12951437
17_198698 rs11869174
17_206962 rs11657163
GI_41393558-I KIF1B chr1 10270763 97892 1_10270386 rs3828081 KIF1B 2 kb upstream
1_10307453 rs4240911 KIF1B intron
1_10438687 rs1536262 KIF1B 3’UTR
GI_4506738-S RPS6KB2 chr11 67195934 6945 11_67196237 rs1476792 RPS6KB2 intron
11_67204342 rs12787021 PTPRCAP intron
11_67213956 rs2109123
11_67253564 rs7110021
11_67258805 rs751567
11_67264679 rs2276120
GI_15451941-S UBA52 chr19 18682613 5657 19_18499151 rs1059022
19_18499238 rs1804826
19_18715154 rs72995445 CRLF1 intron
19_18859680 rs11085244

Gene symbols and coordinates for the ten transcripts that were detected as being potentially cis-regulated by SNPs in our covariance kernel. The closest SNPs to each gene are listed