chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7122158811122158812GC59GENIChomozygous115860288
7122160865122160866GC65GENICheterozygous115860290
7122160978122160979GA113GENICheterozygous115860292
7122161059122161060TA69GENICheterozygous115860294
7122161259122161260TC39GENICheterozygous115860296
7122161750122161751GA25GENIChomozygous115860298
7122164056122164057TC71GENIChomozygous115860300
7122164378122164379CT106GENICheterozygous115860302
7122164404122164405AG98GENICheterozygous115860304
7122164552122164553TC40GENICheterozygous115860306
7122165143122165144AT18GENIChomozygous115860308
7122166143122166144CT38GENIChomozygous115860310
7122166660122166661CT19GENIChomozygous115860312
7122166850122166851TC38GENIChomozygous115860314
7122166853122166854AG38GENICpossibly homozygous115860316
7122173675122173676AG38GENIChomozygous115860318