chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185459540254595403GA31GENIChomozygous110539608
185459543454595435AG20GENIChomozygous110539610
185459573254595733AG29GENIChomozygous110356804
185459590854595909GA32GENIChomozygous110539614
185459980854599809GA14GENIChomozygous110539616
185460117754601178GT36GENIChomozygous110356846
185460204654602047TA30GENIChomozygous110356860
185460255054602551TC19GENIChomozygous110539618
185460263454602635AT14GENIChomozygous110356864
185460389154603892TC13GENIChomozygous110356876
185460535454605355CT18GENIChomozygous110356886
185460668454606685AG30GENIChomozygous110356892
185460802154608022GC16GENIChomozygous110356906
185460837354608374GA22GENIChomozygous110539620
185460936354609364TC23GENIChomozygous110356913
185460954354609544AG13GENIChomozygous110539622
185461125654611257GT20GENIChomozygous110654941
185461186254611863GA20GENIChomozygous110539624
185461263954612640TG24GENICpossibly homozygous110539626
185461474954614750TC18GENIChomozygous110356927