chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87969167579691676TA20GENIChomozygous116844704
87969399779693998CT29GENIChomozygous117948446
87969554079695541CA22GENICpossibly homozygous117948447
87969569879695699TC23GENICpossibly homozygous116844706
87969834379698344AC25GENIChomozygous116844708
87969864879698649TC29GENIChomozygous117948448
87969871879698719GT30GENIChomozygous117948449
87969916279699163AG26GENIChomozygous117948450
87970024179700242AG37GENIChomozygous117928479
87970029579700296TG31GENICpossibly homozygous117948451
87970379179703792TC17GENIChomozygous118119812
87970516179705162CT30GENICpossibly homozygous117948452
87970576179705762CT27GENIChomozygous117948453
87970589479705895AG37GENIChomozygous116844710
87970635779706358GT23GENICpossibly homozygous117948454
87970700679707007CT26GENIChomozygous117948456
87970700779707008CG27GENIChomozygous117948457
87970765479707655CT30GENIChomozygous117948458
87970844079708441AG10GENIChomozygous116844713
87971442479714425TC27GENIChomozygous116844715
87971445279714453TG29GENIChomozygous117948459
87971450279714503GT29GENIChomozygous116844716
87969989179699892TC30GENIChomozygous118104443
87969986379699864GT26GENIChomozygous118104441