chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109021144190211442GA28GENIChomozygous68165194
109021235690212357GA24GENIChomozygous68165197
109021417790214178CT22GENIChomozygous68455203
109021491290214913TA26GENIChomozygous68165200
109021515490215155GA34GENIChomozygous68165203
109021696190216962TC27GENIChomozygous68165206
109021990690219907CA18GENIChomozygous68165210
109021993590219936CG22GENIChomozygous68165213
109021994090219941TG22GENIChomozygous68165216
109021994590219946CA23GENIChomozygous68165219
109021995190219952CA19GENIChomozygous68165222
109022031190220312GA37GENIChomozygous68165225
109022155490221555AC17GENICpossibly homozygous68165228
109022178290221783AG26GENIChomozygous68165231
109022243490222435TC27GENIChomozygous68165234
109022272390222724CT24GENICpossibly homozygous68165237
109022302390223024AG22GENIChomozygous68165240
109022416190224162CT22GENIChomozygous68165246
109022417390224174AG24GENIChomozygous68165249
109022603890226039TG23GENICpossibly homozygous68165253
109022608090226081AG21GENIChomozygous68165256
109022669690226697TA22GENIChomozygous68455206
109022764090227641CA16GENIChomozygous68455209
109023304490233045TC38GENIChomozygous68165277