chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1178141576178141577GA23GENIChomozygous120841936
1178142248178142249CG24GENIChomozygous108403117
1178144831178144832AG19GENIChomozygous108403123
1178145385178145389ATCT24GENIChomozygous127459884
1178149361178149362AG19GENIChomozygous120841944
1178154840178154841GA20GENIChomozygous108403137
1178155559178155560GA29GENIChomozygous108403139
1178155829178155830AG14GENIChomozygous120841946
1178165649178165650GA19GENICpossibly homozygous120841948
1178182617178182618AC20GENIChomozygous108403173
1178183270178183271CA15GENIChomozygous120841950
1178183450178183451CT21GENIChomozygous108403175
1178157137178157138CT25GENIChomozygous125529919
1178180794178180812TTGACTAGCTGGCGTTCC24GENIChomozygous135286991
1178184608178184609TA21GENIChomozygous108403179
1178185097178185098GT19GENIChomozygous108403183
1178185383178185383G19GENIChomozygous127459897
1178186401178186402AG21GENIChomozygous108403189
1178187071178187071C12GENIChomozygous127459899
1178187947178187948GA24GENIChomozygous108403191
1178188520178188521CT24GENIChomozygous120841952
1178189756178189756GCCC3GENIChomozygous135286992
1178191316178191317CT22GENIChomozygous120841954
1178195556178195557A15GENICpossibly homozygous127459901
1178191411178191412TC23GENIChomozygous108403195
1178191789178191790TA32GENIChomozygous108403199
1178196324178196325AC23GENIChomozygous108403207