chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34632746746327468GA17GENIChomozygous788977062
34632800646328007AG19GENIChomozygous788977063
34632844746328448CA25GENIChomozygous788977064
34632878946328790CT20GENIChomozygous788977065
34632894746328948CT28GENIChomozygous788977066
34632896346328964AG25GENIChomozygous788977067
34632946946329470GT18GENIChomozygous788977068
34633021546330216TA23GENIChomozygous788977069
34633045446330455GA21GENIChomozygous788977070
34633095346330954GA17GENIChomozygous788977071
34633115346331154AG11GENIChomozygous788977072
34633631246336313TC21GENIChomozygous788977073
34633638346336384TG29GENIChomozygous788977074
34633742646337427AC27GENIChomozygous788977075
34633904246339043AG25GENIChomozygous788977076
34633938046339381TC24GENIChomozygous788977077
34634092946340930CT28GENIChomozygous788977078
34634136046341361CT22GENIChomozygous788977079
34634192146341922AG15GENIChomozygous788977080
34634200946342010GT28GENIChomozygous788977081
34634218446342185TC29GENIChomozygous788977082
34634448746344488AT24GENIChomozygous788977083
34634632146346322CT22GENIChomozygous788977084
34634656446346565AG15GENIChomozygous788977085
34634845946348460TC9GENIChomozygous788977086
34634864846348649TA5GENIChomozygous788977087
34634973746349738AG29GENIChomozygous788977088
34634998246349983TA16GENIChomozygous788977089
34635100646351007AG20GENIChomozygous788977090
34635180346351804TC20GENIChomozygous788977091
34635198746351988CG26GENIChomozygous788977092
34635198846351989AT26GENIChomozygous788977093
34635206546352066AC28GENICheterozygous788977094
34635456446354565TA14GENIChomozygous788977095
34635630446356305TC29GENICheterozygous788977096
34635630946356310AG27GENICheterozygous788977097
34635791146357912GA16GENIChomozygous788977098
34635826746358268CT9GENIChomozygous788977099