chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
89602034296020343GA25GENIChomozygous116588683
89602060296020603TC18GENIChomozygous116588685
89602629496026295CA8GENIChomozygous116853854
89602630496026305AC9GENICpossibly homozygous118090323
89602655996026560AC12GENIChomozygous116588697
89602810296028103AG18GENIChomozygous116588699
89603068396030684TC16GENIChomozygous116588701
89603221796032218TC12GENIChomozygous116588707
89603587496035875CT6GENIChomozygous116588711
89603653096036531AG22GENIChomozygous116588713
89603870396038704AT5GENIChomozygous116588715
89603964296039643AG22GENIChomozygous116588717
89603990596039906AG21GENIChomozygous116588719
89604262696042627GC25GENIChomozygous116588721
89604801596048016TA3GENIChomozygous116588727
89604805396048054AG4GENIChomozygous116588729
89605579796055798TC17GENIChomozygous116588737
89605964196059642AG16GENIChomozygous116588739
89606002696060027TC13GENIChomozygous116588741
89606003896060039CT13GENIChomozygous116588743
89606292096062921CT21GENIChomozygous116588747
89606380496063805CT15GENICpossibly homozygous117911669
89606489196064892TA10GENIChomozygous116588751
89607182296071823TC12GENIChomozygous116588765
89607274696072747TA20GENIChomozygous116588769
89607431396074314AC20GENIChomozygous116588771
89607827096078271TC15GENIChomozygous116588779
89607431496074315AT20GENIChomozygous116588773
89607508796075088GA17GENIChomozygous116588777
89607903196079032CT10GENIChomozygous116588781
89608114096081141GT16GENIChomozygous117167569
89608581096085811TC14GENIChomozygous116588785
89608749396087494GA16GENIChomozygous116588787
89608760196087602CT15GENIChomozygous116588789
89608775196087752TC21GENIChomozygous116588791