chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135229492135229493CG9GENIChomozygous114993656
6135230368135230369TC13GENIChomozygous114993657
6135232195135232196AG12GENIChomozygous114993658
6135233120135233121CT23GENICpossibly homozygous114993659
6135234256135234257AG21GENIChomozygous114993660
6135234917135234918CT21GENIChomozygous114993661
6135235176135235177AT22GENIChomozygous114993662
6135235997135235998TC28GENIChomozygous114993663
6135236298135236299AG9GENIChomozygous114993664
6135236528135236529TA21GENIChomozygous114993665
6135239227135239228AG30GENIChomozygous114993669
6135239399135239400AG26GENIChomozygous114993670
6135241229135241230CT22GENIChomozygous114993671
6135241383135241384AG29GENIChomozygous114993672
6135241775135241776TA23GENIChomozygous114993673
6135243495135243496GA39GENIChomozygous114993674
6135243844135243845TA24GENIChomozygous114993675
6135244521135244522TC39GENIChomozygous114993676
6135245124135245125CT20GENIChomozygous114993677
6135245219135245220AG20GENIChomozygous114993678
6135245396135245397CT17GENIChomozygous114993679
6135245922135245923AT24GENIChomozygous114993680
6135247178135247179CT27GENIChomozygous114993681
6135247311135247312TG26GENIChomozygous114993682
6135248083135248084TC33GENIChomozygous114993683
6135249456135249457CG29GENIChomozygous114993684
6135250738135250739TC4GENIChomozygous114993686
6135255197135255198AT20GENIChomozygous114993690
6135256489135256490GA23GENIChomozygous114993691
6135256558135256559GA33GENIChomozygous114993692
6135257675135257676TC33GENIChomozygous114993694