chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3108264300108264301C36GENIChomozygous136582745
3108264708108264710CC48GENIChomozygous136582746
3108265196108265197AG49GENIChomozygous136785088
3108266118108266119AC52GENIChomozygous136785090
3108266586108266587G38GENIChomozygous136582747
3108269058108269059AC54GENICpossibly homozygous136785095
3108270149108270150AG49GENIChomozygous136785096
3108270484108270485GC55GENIChomozygous136785097
3108270641108270642GT66GENIChomozygous136785098
3108276223108276224AC65GENIChomozygous146718646
3108267416108267417G53GENIChomozygous146696466
3108270002108270002C41GENIChomozygous146696467
3108267418108267419GA54GENIChomozygous146718641
3108269862108269863CT47GENIChomozygous146718642
3108273208108273209GA52GENIChomozygous146718643
3108276120108276121CT58GENIChomozygous146718644
3108276219108276220TA64GENIChomozygous146718645
3108276622108276623TC55GENIChomozygous136785101
3108280291108280292CA46GENIChomozygous146718647
3108282009108282010CT51GENIChomozygous136785108
3108282190108282191TA44GENIChomozygous141525882