chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18444641884446419T-28GENIChomozygous60748057
18444694984446950AG31GENICpossibly homozygous61452907
18445474584454746CA25GENIChomozygous61452910
18445694284456943TG15GENIChomozygous61452911
18446148684461487GA23GENIChomozygous61452912
18446192884461929GT14GENICpossibly homozygous61452913
18446319884463199G-6GENICheterozygous62551943
18446817984468180TC27GENICpossibly homozygous61452914
18447347584473476GA10GENIChomozygous60748058
18447349184473492AG8GENIChomozygous60748059
18447409084474093TTT---13GENICheterozygous61452915
18447409184474093TT--13GENICheterozygous61885555
18447489384474895TT--6GENICheterozygous62138596
18447489484474895T-6GENICheterozygous62138597
18447932384479324GT18GENIChomozygous61452916
18448010384480105TT--13GENICheterozygous61885565
18448010484480105T-13GENICpossibly homozygous62260652
18448011684480117AAT15GENIChomozygous61452917
18448620484486210GCTCAC------4GENIChomozygous62228039
18448887184488883ACACACACACAC------------4GENIChomozygous61452920
18448893284488933AAAGGGGG8GENIChomozygous60748080
18448900884489009AG16GENICpossibly homozygous61452921
18448934384489344G-14GENIChomozygous60748084
18448937684489377AG17GENIChomozygous60748085