chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2066112886611289GGT12GENICpossibly homozygous768618954
2066113726611373AG8GENICpossibly homozygous670039473
2066114646611465AT5GENIChomozygous670039474
2066114656611466AC5GENIChomozygous670039475
2066115976611602TTTCG-----11GENIChomozygous768618955
2066116886611689TC11GENIChomozygous670039476
2066124006612401GC12GENIChomozygous670039477
2066127706612771GA7GENIChomozygous670039478
2066129966612997CT15GENICheterozygous670039479
2066130516613052AC8GENIChomozygous670039480
2066131206613121AG18GENIChomozygous670039481
2066135346613535CA15GENICpossibly homozygous670039482
2066135556613556AG13GENICpossibly homozygous670039483
2066146516614652CT17GENICpossibly homozygous670039484
2066148406614844ATTT----4GENICheterozygous768618956
2066151896615190C-7GENIChomozygous768618957
2066152656615266AG8GENICpossibly homozygous670039485
2066153816615382GA12GENIChomozygous670039486
2066154536615454CCA12GENIChomozygous768618958