chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
178958566189585662TG9GENIChomozygous968251694
178958628889586289AG11GENIChomozygous968251695
178960054189600542AG9GENIChomozygous968251696
178960444989604450TC21GENIChomozygous968251697
178960506889605069CT10GENIChomozygous968251698
178960529389605294GA17GENIChomozygous968251699
178960709089607091TA10GENIChomozygous968251700
178962055389620554CA17GENIChomozygous968251701
178962621589626216GT5GENIChomozygous968251702
178962790889627909CG13GENIChomozygous968251703
178963569789635698GA12GENIChomozygous968251704
178963806789638068TC11GENIChomozygous968251705
178963869789638698CT13GENIChomozygous968251706
178963943889639439TG20GENIChomozygous968251707
178964746889647469GA13GENIChomozygous968251708
178964805489648055AG18GENIChomozygous968251709
178964918589649186AG13GENIChomozygous968251710
178965263289652633GA9GENIChomozygous968251711
178965481389654814GA17GENIChomozygous968251712
178966028589660286TC7GENIChomozygous968251713
178966231989662320GA15GENIChomozygous968251714
178966253189662532GC17GENIChomozygous968251715
178966448789664488GT4GENIChomozygous968251716
178966452189664522AG9GENIChomozygous968251717
178966563589665636CG13GENIChomozygous968251718