Table 1.

Shared descriptors of differentially expressed imprinted genes in LOS fetuses

Rank	Descriptor	No. of genes	Associated imprinted genes	P value
1	Beckwith–Wiedemann syndrome	13	CDKN1C, H19, IGF2, IGF2R, KCNQ1, NAP1L4, PEG3, PHLDA2, PLAGL1, SLC22A18, SNRPN, TSPAN32, TSSC4	1.00 × 10−16
2	Growth/size/body phenotype	34	ANO1, CD81, CDKN1C, COMMD1, DCN, DHCR7, DIO3, DLK1, DNMT1, GATM, GLIS3, GNAS, H19, IGF2, IGF2R, KCNQ1, LIN28B, MAGEL2, MEST, PDE10A, PDE4D, PEG10, PEG3, PHLDA2, PLAGL1, PON3, RASGRF1, RB1, RTL1, SLC22A3, SNRPN, TCEB3, TP73, UBE3A	1.00 × 10−16
3	Cellular phenotype	30	AMPD3, AXL, CDKN1C, DCN, DIO3, DLK1, DNMT1, GNAS, H19, IGF2, IGF2R, L3MBTL1, MAGEL2, MEST, NDN, PDE4D, PEG10, PEG3, PHLDA2, PLAGL1, PON2, PON3, RASGRF1, RB1, SGCE, SLC22A3, SNRPN, TCEB3, TP73, UBE3A	2.11 × 10−15
4	Tumors	32	AMPD3, ANO1, AXL, BLCAP, CALCR, CD81, CDKN1C, DCN, DIO3, DLK1, DNMT1, GNAS, H19, IGF2, IGF2R, L3MBTL1, NAP1L4, NDN, NNAT, NTM, PEG3, PLAGL1, QPCT, RB1, SLC22A18, SLC22A3, TCEB3, TFPI2, TP73, TSPAN32, UBE3A, WIF1	1.02 × 10−14