chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
162104868521048686TTTTTTG19GENIChomozygous47741285
162104901021049011TTCACACACA12GENIChomozygous47741289
162104929621049297T-5GENIChomozygous47882589
162104948021049481CCCCG3GENIChomozygous47329452
162105044521050446A-11GENICpossibly homozygous47329456
162105127121051272GT25GENIChomozygous47741291
162105343421053436AA--10GENICheterozygous47329458
162105343521053436A-10GENICpossibly homozygous47741293
162105375821053759AACTG17GENIChomozygous47329460
162105503221055034GG--5GENIChomozygous47329470
162105870621058707CCT7GENICpossibly homozygous47329480
162105891321058914C-11GENIChomozygous47329484
162105880521058806CCT7GENIChomozygous47627458
162106228821062289CT13GENIChomozygous47741295
162107440421074405GGT14GENICpossibly homozygous47329498
162106215321062154GGA3GENICheterozygous47924427
162106850121068502CCAAA3GENICheterozygous47986768