chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1253220779253220780GT22GENIChomozygous108613421
1253220914253220915T21GENIChomozygous131266595
1253228176253228177AG20GENIChomozygous120604013
1253223244253223245CT21GENIChomozygous120604009
1253244036253244043TTATTCC19GENIChomozygous131266597
1253247873253247873T14GENIChomozygous131266598
1253253477253253478TC22GENIChomozygous108613428
1253237278253237279AT11GENIChomozygous125493657
1253238542253238543TC18GENIChomozygous108613423
1253243043253243044CT18GENIChomozygous120880331
1253244666253244667CT23GENIChomozygous108613426
1253253186253253187CT14GENIChomozygous108613427
1253253590253253591AG17GENIChomozygous108613429
1253257836253257837CT20GENIChomozygous120890814
1253258407253258407TT23GENIChomozygous131266599
1253260087253260088TC24GENIChomozygous120604015
1253261951253261952GT8GENIChomozygous109020578
1253263100253263101AG16GENIChomozygous120604017
1253265098253265099AG22GENIChomozygous108613441
1253272661253272662CT13GENIChomozygous120880334
1253272718253272719C12GENIChomozygous131266600