chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135230368135230369TC13GENIChomozygous114993657
6135232195135232196AG9GENIChomozygous114993658
6135233120135233121CT23GENIChomozygous114993659
6135234256135234257AG23GENIChomozygous114993660
6135234917135234918CT26GENIChomozygous114993661
6135235176135235177AT18GENIChomozygous114993662
6135235997135235998TC10GENIChomozygous114993663
6135236298135236299AG7GENIChomozygous114993664
6135237397135237398AG18GENIChomozygous114993666
6135238012135238013CT16GENIChomozygous114993668
6135238422135238423TG8GENICheterozygous126367377
6135239227135239228AG12GENIChomozygous114993669
6135239399135239400AG26GENIChomozygous114993670
6135241229135241230CT20GENIChomozygous114993671
6135241775135241776TA21GENIChomozygous114993673
6135243495135243496GA22GENIChomozygous114993674
6135243844135243845TA8GENIChomozygous114993675
6135244521135244522TC20GENIChomozygous114993676
6135245124135245125CT14GENIChomozygous114993677
6135245219135245220AG24GENIChomozygous114993678
6135245396135245397CT18GENIChomozygous114993679
6135245922135245923AT20GENIChomozygous114993680
6135247178135247179CT22GENIChomozygous114993681
6135247311135247312TG10GENIChomozygous114993682
6135248083135248084TC28GENIChomozygous114993683
6135249456135249457CG24GENIChomozygous114993684
6135250372135250373TA11GENIChomozygous114993685
6135250738135250739TC23GENIChomozygous114993686
6135250754135250755GC17GENIChomozygous114993687
6135255197135255198AT6GENIChomozygous114993690
6135256489135256490GA22GENIChomozygous114993691
6135256558135256559GA17GENIChomozygous114993692
6135257675135257676TC25GENIChomozygous114993694
6135258447135258448CA4GENIChomozygous114993696
6135251855135251856AG3GENICheterozygous126485318