chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265506921265506922CT52GENIChomozygous108637134
1265507749265507750TG48GENIChomozygous108637135
1265510327265510328AC38GENIChomozygous108637136
1265510911265510912AG41GENIChomozygous108637137
1265510999265511000TC48GENIChomozygous108637138
1265512099265512100CT54GENIChomozygous108637139
1265512411265512412TC57GENIChomozygous108637140
1265513478265513479TC40GENIChomozygous108637141
1265514233265514234GA49GENIChomozygous108637142
1265516163265516164AC57GENICpossibly homozygous108637143
1265517331265517332GA42GENIChomozygous108637144
1265519549265519550GA48GENIChomozygous108637145
1265520577265520578A8GENIChomozygous127508881
1265513830265513835AAAAC36GENIChomozygous127508879
1265518514265518515A52GENIChomozygous127508880
1265521505265521505T45GENIChomozygous127508883
1265523226265523226GGGGAG26GENIChomozygous127508884
1265524821265524822TG45GENIChomozygous108637146
1265527947265527948AG63GENIChomozygous108637147
1265528073265528074A39GENIChomozygous127508885
1265529410265529411TC44GENIChomozygous108637148
1265529578265529579CT48GENIChomozygous108637149
1265530494265530495TC63GENIChomozygous108637150
1265530503265530504CG54GENIChomozygous108637151
1265530772265530773CT57GENIChomozygous108637152
1265533648265533649T25GENIChomozygous127508886
1265520610265520610C7GENIChomozygous131784770
1265534192265534193TG3GENIChomozygous125327320