chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
91602451316024514AC20GENIChomozygous601297404
91602484416024845CG22GENIChomozygous601297405
91602788816027889TC35GENIChomozygous602389518
91602857416028575TA17GENIChomozygous601297406
91602949416029495AAG20GENIChomozygous731515483
91603178416031785TC27GENIChomozygous602389519
91603193516031936CCA31GENIChomozygous731515484
91603193716031938GC32GENIChomozygous602389520
91603224216032243GA29GENIChomozygous601297407
91603378516033788TCT---4GENICheterozygous731515485
91603403916034040CT23GENIChomozygous602389521
91603423716034238T-5GENIChomozygous731515486
91603583616035837GA22GENIChomozygous602389522
91603630716036308TTA19GENIChomozygous731515487
91603780416037822AAAAAAAAAAAAAAAAAT------------------32GENICheterozygous731515488
91604228516042286CCCCTCTTCTGGCCTG24GENIChomozygous731515489
91604288516042886TTTG18GENICpossibly homozygous731515491
91604288516042886TTTGTGTG18GENICheterozygous731515493
91604451116044512GT31GENIChomozygous601297408
91604486116044862AAACACACAC6GENICheterozygous731515495
91604486116044862AAACACACACACACAC6GENICheterozygous731515496
91604724116047242CG9GENIChomozygous602389523
91604943816049439TA33GENIChomozygous602389524
91605076216050766GTGG----12GENIChomozygous731515497
91605120716051208TC21GENIChomozygous601297409
91605261716052618TC38GENIChomozygous601297410
91605277516052776AG29GENIChomozygous601297411
91605317616053177CT31GENIChomozygous602389525
91605585216055854AA--24GENIChomozygous731515498
91605707416057076CA--6GENICheterozygous731515499
91605762616057627AG26GENIChomozygous601297412
91605873616058737TC29GENIChomozygous601297413
91605926316059264GA17GENICpossibly homozygous601297414