chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975309103975310CG35GENIChomozygous61733095
1103975892103975893AAC15GENIChomozygous61733097
1103976805103976807TG--19GENIChomozygous61733099
1103977911103977912AG11GENIChomozygous61733101
1103977946103977947CCTTTCTTTTCT7GENICpossibly homozygous61733105
1103978035103978036CCT7GENIChomozygous61733107
1103979378103979379GA26GENIChomozygous61733109
1103980780103980781CT17GENIChomozygous61733110
1103981157103981158TC32GENIChomozygous61733112
1103981201103981202CA29GENIChomozygous61733114
1103981242103981243TC26GENIChomozygous61733116
1103981729103981731GT--14GENICheterozygous62147687
1103981778103981779TG17GENIChomozygous61733118
1103981782103981783AC18GENIChomozygous61733120
1103981798103981799T-17GENIChomozygous61733122
1103981911103981912AG26GENICpossibly homozygous61733124
1103982160103982161CT42GENIChomozygous61733126
1103982675103982676GA28GENIChomozygous61733128
1103982941103982949TTGTTTTG--------12GENICpossibly homozygous61299649
1103982956103982957GA13GENIChomozygous62147688
1103982958103982960GG--13GENIChomozygous60780361
1103983211103983212AT22GENIChomozygous61733130
1103983522103983523AG29GENIChomozygous61733132
1103983926103983929AGG---27GENIChomozygous61733134
1103984217103984218GGGTTAGTCCA14GENIChomozygous62147690