chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1127716578127716579TC23GENIChomozygous108223668
1127716588127716589GC15GENIChomozygous108223670
1127716598127716599TC8GENIChomozygous108223672
1127716601127716602GA8GENIChomozygous108223674
1127721106127721107AC9GENIChomozygous108223676
1127736286127736287AG15GENICheterozygous108223678
1127736361127736362CT22GENICheterozygous108223680
1127736370127736371AG19GENICheterozygous108223682
1127736384127736385CA15GENICheterozygous108223684
1127736393127736394TG15GENICheterozygous108223686
1127736404127736405TC15GENICpossibly homozygous108223688
1127737300127737301GA46GENICheterozygous108742406
1127746616127746617GA12GENICheterozygous108742407
1127746633127746634AG16GENICheterozygous108223694
1127736261127736262GA13GENICheterozygous108926938
1127758036127758037CT19GENIChomozygous108223696
1127771685127771686TG4GENIChomozygous108223698
1127777610127777611AC18GENICheterozygous108926940