chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1171717169171717170CCT12GENICpossibly homozygous705664198
1171718056171718057GA20GENIChomozygous559793244
1171718517171718518GC11GENIChomozygous561894956
1171719640171719641GA23GENIChomozygous561894957
1171719975171719976CT32GENIChomozygous559793245
1171720545171720557GTGTGTGTGTGT------------14GENICheterozygous705664201
1171720547171720557GTGTGTGTGT----------14GENICheterozygous705664202
1171722684171722694ACACAGACAC----------43GENIChomozygous705664203
1171723538171723539GGAGAGAC21GENIChomozygous705664204
1171723594171723596GA--25GENIChomozygous705664206
1171724267171724268GC11GENIChomozygous561894958
1171725400171725410GAGAGAGAGA----------8GENIChomozygous705664207
1171725897171725898TA28GENIChomozygous559793246
1171726218171726219T-6GENIChomozygous705664209
1171729382171729383AC16GENIChomozygous559793247