chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1253220779253220780GT12GENIChomozygous108613421
1253226383253226384AG2GENIChomozygous120476979
1253238542253238543TC16GENIChomozygous108613423
1253243030253243031AG46GENIChomozygous108613424
1253244536253244537CT22GENIChomozygous108613425
1253244666253244667CT27GENIChomozygous108613426
1253253186253253187CT28GENIChomozygous108613427
1253253477253253478TC39GENIChomozygous108613428
1253253590253253591AG54GENIChomozygous108613429
1253254264253254265TC53GENIChomozygous108613430
1253254279253254280AT58GENIChomozygous108613431
1253254815253254816GA23GENIChomozygous108613432
1253258366253258367GA24GENIChomozygous108613435
1253262738253262739CT25GENIChomozygous108613439
1253264953253264954GA34GENIChomozygous108613440
1253265098253265099AG36GENIChomozygous108613441
1253266093253266094CT18GENIChomozygous108613442
1253267064253267065CT35GENIChomozygous108613443
1253272191253272192AG20GENIChomozygous108613444
1253274650253274651TC25GENIChomozygous108613446