chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
109021144190211442GA33GENIChomozygous68165194
109021235690212357GA51GENICpossibly homozygous68165197
109021417790214178CT46GENIChomozygous68455203
109021491290214913TA39GENIChomozygous68165200
109021515490215155GA47GENIChomozygous68165203
109021696190216962TC26GENIChomozygous68165206
109021990690219907CA17GENIChomozygous68165210
109021993590219936CG7GENIChomozygous68165213
109021994090219941TG7GENIChomozygous68165216
109021994590219946CA7GENIChomozygous68165219
109021995190219952CA6GENIChomozygous68165222
109022031190220312GA17GENIChomozygous68165225
109022155490221555AC27GENICpossibly homozygous68165228
109022178290221783AG30GENIChomozygous68165231
109022243490222435TC46GENIChomozygous68165234
109022272390222724CT30GENIChomozygous68165237
109022302390223024AG32GENIChomozygous68165240
109022353190223532CT14GENICpossibly homozygous68165243
109022416190224162CT39GENIChomozygous68165246
109022417390224174AG38GENIChomozygous68165249
109022603890226039TG21GENICheterozygous68165253
109022608090226081AG20GENIChomozygous68165256
109022669690226697TA31GENICpossibly homozygous68455206
109022764090227641CA20GENIChomozygous68455209
109023304490233045TC44GENIChomozygous68165277