chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106974786106974787CT20GENIChomozygous610387760
10106975785106975786TTCC18GENIChomozygous734120855
10106976030106976031CA11GENIChomozygous612396959
10106976031106976032AC11GENIChomozygous612396960
10106979282106979283GGGTGTGTGTGTGTGT24GENICheterozygous734120858
10106979283106979289GTGTGT------24GENICheterozygous734120856
10106979287106979289GT--24GENICheterozygous734120857
10106985083106985084AATG17GENICheterozygous734120860
10106985084106985086TG--17GENICheterozygous734120859
10106993450106993452AA--17GENICheterozygous734120864
10106995085106995087GT--12GENICheterozygous734120865
10107014077107014080TTT---18GENICheterozygous734120866
10107014078107014080TT--18GENICheterozygous734120867
10107016315107016316GGA9GENICheterozygous734120869
10107016316107016317A-9GENICheterozygous734120868