chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1103975309103975310CG31GENIChomozygous61733095
1103975892103975893AAC22GENIChomozygous61733097
1103976805103976807TG--49GENIChomozygous61733099
1103977911103977912AG41GENIChomozygous61733101
1103977942103977943CCT23GENICheterozygous61733103
1103977946103977947CCTTTCTTTTCT25GENIChomozygous61733105
1103978035103978036CCT31GENIChomozygous61733107
1103979378103979379GA58GENIChomozygous61733109
1103980780103980781CT41GENIChomozygous61733110
1103981157103981158TC43GENIChomozygous61733112
1103981201103981202CA44GENIChomozygous61733114
1103981242103981243TC37GENIChomozygous61733116
1103981778103981779TG26GENIChomozygous61733118
1103981782103981783AC29GENIChomozygous61733120
1103981798103981799T-31GENIChomozygous61733122
1103981911103981912AG38GENIChomozygous61733124
1103982160103982161CT36GENICpossibly homozygous61733126
1103982675103982676GA34GENIChomozygous61733128
1103982941103982949TTGTTTTG--------11GENIChomozygous61299649
1103982943103982944G-11GENIChomozygous60780359
1103982948103982949G-12GENICheterozygous60780360
1103982958103982960GG--11GENIChomozygous60780361
1103983211103983212AT31GENIChomozygous61733130
1103983522103983523AG30GENIChomozygous61733132
1103983926103983929AGG---37GENIChomozygous61733134
1103984221103984222GA20GENICheterozygous61733136
1103984318103984319AG61GENICheterozygous60780362
1103984364103984365TC67GENICheterozygous60780363
1103984546103984547TC50GENICheterozygous61733138