chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2210394186210394187GC53GENICpossibly homozygous110223085
2210395945210395946TC44GENIChomozygous110223086
2210400339210400339C22GENICpossibly homozygous127732589
2210400899210400900AG51GENIChomozygous110223088
2210402120210402121AG43GENIChomozygous110223089
2210404084210404085TC39GENIChomozygous110223090
2210404542210404543T45GENIChomozygous127732590
2210404690210404691GA63GENIChomozygous110223091
2210406992210406993AG57GENIChomozygous110223092
2210408095210408096GA45GENIChomozygous110223093
2210410268210410269GA42GENIChomozygous110223094
2210411408210411409TC35GENIChomozygous110223095
2210411976210411977CT63GENIChomozygous110223096
2210412217210412218CG59GENIChomozygous110223097
2210413158210413159AT53GENIChomozygous110223098
2210413227210413228TC53GENIChomozygous110223099
2210413369210413370TA53GENIChomozygous110223100