chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135325764135325765AG16GENICpossibly homozygous70702909
6135331089135331090TG7GENIChomozygous71107427
6135331305135331306TC6GENIChomozygous70702921
6135340652135340653CA36GENIChomozygous70702933
6135340679135340680CG34GENIChomozygous70702936
6135340746135340747CG26GENIChomozygous70702939
6135340748135340749CT26GENIChomozygous70702942
6135357010135357011AT4GENIChomozygous70702978
6135361650135361651AG30GENICpossibly homozygous71107435
6135380397135380398AG18GENIChomozygous70703083
6135389553135389554GA27GENIChomozygous71107439
6135331726135331727GT5GENIChomozygous71840803
6135365511135365512GA15GENICheterozygous71840806