chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1234959285234959286T-13GENIChomozygous61609503
1234959342234959343GA16GENIChomozygous61609504
1234960295234960296A-17GENIChomozygous61609505
1234960790234960791CT22GENIChomozygous61609507
1234960821234960822G-27GENIChomozygous61609508
1234961134234961135AG22GENIChomozygous61609509
1234961941234961942CCA14GENIChomozygous61609510
1234962751234962752GGA25GENIChomozygous61609511
1234962767234962768GGA29GENIChomozygous61609512
1234963862234963865GGG---16GENIChomozygous61609513
1234964705234964706AAC20GENIChomozygous61609514
1234964808234964809TG23GENIChomozygous61609515
1234965730234965731TTC10GENIChomozygous61609516
1234965739234965740TC9GENIChomozygous62556795
1234966388234966389GC18GENIChomozygous61609517
1234966625234966626GA21GENIChomozygous61609518
1234966679234966680CT24GENIChomozygous61609519
1234966980234966981TC22GENIChomozygous61609520
1234967095234967115GTGTGTGTGTGTGTGTGTTG--------------------16GENICpossibly homozygous62276173
1234967138234967139CT24GENICheterozygous62104730
1234967144234967145TTG24GENICheterozygous62204141
1234967158234967159GT29GENICheterozygous62104731
1234967176234967178CT--38GENICheterozygous62204143
1234967177234967178TTGGGGGG38GENICheterozygous62204145
1234967180234967181AAG39GENICheterozygous62204147
1234967229234967230TTAAA48GENICheterozygous62204149