chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81615074816150749CG49GENIChomozygous146855792
81615112216151123CT40GENIChomozygous146855793
81615114416151145TC42GENIChomozygous142043812
81615168016151682GG50GENIChomozygous146840789
81615274916152750AG43GENIChomozygous146855794
81615286016152860A53GENIChomozygous146840790
81615294716152947A42GENIChomozygous146840791
81615353416153535AC39GENICpossibly homozygous146855795
81615386116153862CG34GENIChomozygous146855796
81615557516155576GT39GENIChomozygous142043840
81615608916156090GA25GENIChomozygous142043844
81615769416157695GA55GENIChomozygous146855797
81615934216159343TC47GENIChomozygous143389149