chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1253220779253220780GT52GENICpossibly homozygous108613421
1253226385253226386AG15GENIChomozygous109020565
1253237030253237031AT4GENIChomozygous121309714
1253237036253237037AT4GENIChomozygous121309717
1253237040253237041AT4GENIChomozygous121309718
1253230977253230988TAATAGTGCTG58GENIChomozygous127504451
1253237170253237170GA24GENIChomozygous127504452
1253237276253237277TA19GENICpossibly homozygous127584614
1253238542253238543TC51GENIChomozygous108613423
1253243030253243031AG47GENIChomozygous108613424
1253244536253244537CT52GENIChomozygous108613425
1253244666253244667CT48GENIChomozygous108613426
1253253186253253187CT44GENIChomozygous108613427
1253253477253253478TC58GENIChomozygous108613428
1253253590253253591AG48GENIChomozygous108613429
1253254264253254265TC47GENIChomozygous108613430
1253254279253254280AT45GENIChomozygous108613431
1253254815253254816GA48GENIChomozygous108613432
1253255254253255255CG8GENIChomozygous108613433
1253255273253255273TC5GENIChomozygous129845980
1253258366253258367GA45GENIChomozygous108613435
1253258900253258901TC57GENIChomozygous108613436
1253261951253261952GT35GENIChomozygous109020578
1253262265253262266GA51GENIChomozygous108613438
1253262738253262739CT59GENIChomozygous108613439
1253264953253264954GA49GENIChomozygous108613440
1253265098253265099AG36GENIChomozygous108613441
1253266093253266094CT49GENIChomozygous108613442
1253267064253267065CT50GENIChomozygous108613443
1253272191253272192AG43GENIChomozygous108613444
1253272653253272654CT29GENIChomozygous108613445
1253274650253274651TC36GENIChomozygous108613446