chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265506921265506922CT52GENIChomozygous108637134
1265507749265507750TG48GENIChomozygous108637135
1265510327265510328AC67GENIChomozygous108637136
1265510911265510912AG37GENIChomozygous108637137
1265510999265511000TC51GENIChomozygous108637138
1265512099265512100CT56GENIChomozygous108637139
1265512411265512412TC38GENIChomozygous108637140
1265513478265513479TC53GENIChomozygous108637141
1265514233265514234GA48GENICpossibly homozygous108637142
1265516163265516164AC57GENIChomozygous108637143
1265517331265517332GA57GENIChomozygous108637144
1265519549265519550GA65GENIChomozygous108637145
1265520577265520578A6GENIChomozygous127508881
1265513830265513835AAAAC48GENIChomozygous127508879
1265518514265518515A60GENIChomozygous127508880
1265521505265521505T50GENIChomozygous127508883
1265523226265523226GGGGAG29GENIChomozygous127508884
1265524821265524822TG51GENIChomozygous108637146
1265527947265527948AG49GENIChomozygous108637147
1265528073265528074A42GENIChomozygous127508885
1265529410265529411TC58GENIChomozygous108637148
1265529578265529579CT53GENIChomozygous108637149
1265530494265530495TC60GENIChomozygous108637150
1265530503265530504CG57GENIChomozygous108637151
1265530772265530773CT55GENIChomozygous108637152
1265533648265533649T34GENIChomozygous127508886
1265534192265534193TG8GENIChomozygous125327320