chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
35764701057647011GC48GENIChomozygous111580310
35765041457650415GA75GENIChomozygous111910806
35765040457650405GA70GENICpossibly homozygous111910805
35764947157649472GA68GENIChomozygous111910803
35764977857649779GA64GENIChomozygous111910804
35765124357651244CT6GENIChomozygous111910807
35765124657651247GA6GENIChomozygous111910808
35765168357651684TC41GENIChomozygous111910809
35765205857652059TC47GENIChomozygous111580322
35765227457652275AT64GENICpossibly homozygous111910810
35765338357653384AG75GENIChomozygous111580324
35765357757653578GC73GENIChomozygous111910811
35765635157656352TA60GENIChomozygous111910812
35765853657658537TG78GENICpossibly homozygous111910813
35765978857659789AG62GENIChomozygous111580331
35765997157659972TC87GENIChomozygous111580333
35766085757660858TC51GENIChomozygous111580334
35766188557661886CG69GENICpossibly homozygous111580335
35766237357662374CT26GENICheterozygous111910814
35766267857662679AT56GENICpossibly homozygous111910815
35766290057662901AG40GENICheterozygous111910816
35766372457663725TA50GENIChomozygous111580337
35766499857664999TC52GENIChomozygous111580338
35766591757665918AG51GENIChomozygous111910817
35766864357668644AT43GENIChomozygous111580343
35767625657676257TC69GENIChomozygous111580353
35767705457677055CA61GENIChomozygous111910818
35767814157678142CG46GENIChomozygous111580355