chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1198004136198004137TC36GENIChomozygous108496735
1198004195198004196CT44GENICpossibly homozygous108981887
1198004278198004296TGTGTACCACATGTGTTC45GENIChomozygous127472073
1198004427198004428GA49GENIChomozygous108981888
1198004778198004778A50GENIChomozygous131581179
1198004839198004846GGCCCTG48GENIChomozygous131581180
1198005802198005803AG41GENIChomozygous108496741
1198006315198006316AG46GENIChomozygous108496743
1198006354198006355CT51GENIChomozygous108981889
1198006614198006615TC37GENIChomozygous108496745
1198006711198006712AG49GENIChomozygous108496747
1198006781198006782GA56GENICpossibly homozygous108981890
1198007506198007507TC39GENIChomozygous108496749
1198007762198007763TA48GENIChomozygous108496751
1198007973198007974GA40GENIChomozygous108496753
1198009421198009422AG40GENIChomozygous108496755