chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124069554240695543TA12GENIChomozygous50204344
124069595540695956CG19GENICpossibly homozygous50204345
124069787740697878TC16GENIChomozygous50204348
124069816140698162AG7GENIChomozygous50204349
124069866840698669GA13GENICpossibly homozygous50204350
124069875040698751TC14GENIChomozygous50204351
124069902040699021GA15GENICpossibly homozygous50204352
124069985740699863AGAAGG------1INTERGENIChomozygous50204355
124069992040699921GC6INTERGENIChomozygous50204356
124070181940701820GA21INTERGENICpossibly homozygous50204361
124070198240701983T-3INTERGENIChomozygous50204364
124070197840701979CCA4INTERGENIChomozygous50204363
124070198440701985TC3INTERGENIChomozygous50204365
124070245340702454TTA1INTERGENIChomozygous50204370
124070246840702469G-1INTERGENIChomozygous50204371
124070250340702504TC2INTERGENIChomozygous50204372
124070292340702924CT25INTERGENICpossibly homozygous50204373
124070358340703584CCTT5INTERGENICheterozygous50204374
124070441340704414GA21INTERGENICpossibly homozygous50204375
124070910040709101TC12INTERGENIChomozygous50204379