chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185361363553613636AT13GENIChomozygous110353888
185361378053613781C19GENIChomozygous129539375
185361594953615950GA20GENIChomozygous110353890
185361804053618041AG18GENIChomozygous110353892
185361872753618728TC19GENICpossibly homozygous110353894
185361966953619670CT16GENIChomozygous110353896
185362080953620810GA21GENIChomozygous110353898
185362354253623543GT18GENIChomozygous110353900
185362453453624535CT19GENIChomozygous110353902
185362496853624969AG23GENIChomozygous110353904
185362501153625012CA30GENIChomozygous110353906
185362556253625563TC17GENIChomozygous110353908
185361576553615769AAAC11GENIChomozygous129539377
185362109553621095TGAGGC13GENIChomozygous129539378
185362384853623848G22GENIChomozygous129539379
185362652853626529GA17GENIChomozygous110353910
185362676253626763GT27GENIChomozygous110353912
185362704053627041TC21GENIChomozygous110353914
185362778353627783AAAC26GENIChomozygous129539380
185362781653627817A23GENIChomozygous129539381
185362785053627851TG27GENIChomozygous110353916
185362785953627860TC26GENIChomozygous110353918
185362831753628317AA25GENIChomozygous129539382
185362891653628917AG11GENIChomozygous110353920
185362891753628918AG11GENIChomozygous110353922
185363001253630013CA14GENIChomozygous110353924
185363134253631342AT23GENICpossibly homozygous129539383
185363148853631489AG22GENIChomozygous110353926
185363148953631490AG22GENIChomozygous110353928
185363225553632256TA28GENIChomozygous110353930
185363351453633515TC23GENIChomozygous110353932
185363366953633670GA27GENIChomozygous110353934
185364306153643062GA11GENIChomozygous119493771
185363143253631433GT25GENIChomozygous110538290
185364336653643367AG6GENICheterozygous129572730
185364472653644727GT6GENICheterozygous129572733