chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975309103975310CG20GENIChomozygous61733095
1103975892103975893AAC15GENIChomozygous61733097
1103976805103976807TG--22GENIChomozygous61733099
1103977911103977912AG32GENIChomozygous61733101
1103977946103977947CCTTTCTTTTCT23GENICheterozygous61733105
1103978035103978036CCT25GENIChomozygous61733107
1103979378103979379GA19GENIChomozygous61733109
1103980780103980781CT24GENIChomozygous61733110
1103981157103981158TC36GENIChomozygous61733112
1103981201103981202CA32GENIChomozygous61733114
1103981242103981243TC21GENIChomozygous61733116
1103981729103981731GT--19GENICheterozygous62147687
1103981778103981779TG27GENIChomozygous61733118
1103981782103981783AC27GENIChomozygous61733120
1103981798103981799T-28GENIChomozygous61733122
1103981911103981912AG26GENIChomozygous61733124
1103982160103982161CT14GENIChomozygous61733126
1103982675103982676GA16GENIChomozygous61733128
1103982941103982949TTGTTTTG--------20GENIChomozygous61299649
1103982956103982957GA20GENIChomozygous62147688
1103982958103982960GG--21GENIChomozygous60780361
1103983211103983212AT27GENIChomozygous61733130
1103983522103983523AG17GENIChomozygous61733132
1103983926103983929AGG---15GENIChomozygous61733134
1103984217103984218GGGTTAGTCCA19GENICheterozygous62147690
1103984217103984218GGGCTGGTCCA19GENICheterozygous62085404
1103984513103984514TTTA20GENICheterozygous62548810