chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975309103975310CG16GENIChomozygous61733095
1103975892103975893AAC6GENIChomozygous61733097
1103976805103976807TG--21GENIChomozygous61733099
1103977911103977912AG18GENIChomozygous61733101
1103977946103977947CCTTTCTTTTCT5GENICheterozygous61733105
1103978035103978036CCT12GENICpossibly homozygous61733107
1103979378103979379GA28GENIChomozygous61733109
1103980780103980781CT24GENIChomozygous61733110
1103981157103981158TC24GENIChomozygous61733112
1103981201103981202CA21GENIChomozygous61733114
1103981242103981243TC15GENIChomozygous61733116
1103981778103981779TG16GENIChomozygous61733118
1103981782103981783AC16GENIChomozygous61733120
1103981798103981799T-14GENIChomozygous61733122
1103981911103981912AG21GENIChomozygous61733124
1103982160103982161CT15GENIChomozygous61733126
1103982675103982676GA17GENIChomozygous61733128
1103982941103982949TTGTTTTG--------12GENIChomozygous61299649
1103982956103982957GA13GENIChomozygous62147688
1103982958103982960GG--13GENIChomozygous60780361
1103983211103983212AT29GENIChomozygous61733130
1103983522103983523AG30GENIChomozygous61733132
1103983926103983929AGG---32GENIChomozygous61733134
1103984217103984218GGGTTAGTCCA25GENICheterozygous62147690
1103984217103984218GGGCTGGTCCA25GENICheterozygous62085404