chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
16684480766844808GA42GENIChomozygous148662477
16684548366845491GTGTGCGT36GENIChomozygous147891502
16684616766846168CT57GENIChomozygous148662478
16684765666847657AC46GENIChomozygous147915441
16684907966849080T23GENIChomozygous148655904
16684932666849327TC50GENIChomozygous148662479
16685114066851140G9GENIChomozygous147891505
16685118766851187GAGAGAGAAAAAGA15GENIChomozygous148655905
16685119166851191GGGGGGT19GENIChomozygous148655906
16685173266851733CT45GENIChomozygous147915444
16685300366853004TC48GENIChomozygous147915447
16685305366853054G57GENIChomozygous148655907
16685449866854499AG43GENIChomozygous147915450
16685528966855290GC58GENIChomozygous148662480
16685530466855305AG58GENIChomozygous147915452
16685550066855501CT48GENIChomozygous148662481
16685567166855672GA67GENIChomozygous148662482
16685574566855746GT71GENIChomozygous147915453
16685763766857638CT38GENIChomozygous148662483
16685851166858512GA48GENIChomozygous148662484
16686028966860290A28GENIChomozygous148655908
16686029166860296ATATA30GENIChomozygous148655909
16686058266860583GA27GENIChomozygous147915458
16685115066851152GA9GENIChomozygous135410294
16686029566860296AT30GENICheterozygous153832826
16686029566860296A30GENIChomozygous404315289
16686413466864135TG29GENICpossibly homozygous147915461
16686291666862917AC29GENICheterozygous148828124
16686292466862925AC30GENICheterozygous148828125
16686380866863809CA4GENICheterozygous148828126
16686411966864120CT26GENICpossibly homozygous148828127
16686405566864056C19GENICpossibly homozygous148820366
16686405766864102CACACACACACACACACACACACACACACACACACACACACACAC19GENICpossibly homozygous148820367