chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5159590044159590045CT18GENIChomozygous990935207
5159590355159590356AC17GENIChomozygous990935208
5159590356159590357GC17GENIChomozygous990935209
5159590377159590378GA22GENIChomozygous990935210
5159590516159590517AG17GENIChomozygous990935211
5159590543159590544TC13GENIChomozygous990935212
5159590567159590568TC18GENIChomozygous990935213
5159590810159590811GA27GENIChomozygous990935214
5159591041159591042CT10GENIChomozygous990935215
5159591165159591166AG14GENIChomozygous990935216
5159591294159591295GA12GENIChomozygous990935217
5159591492159591493CT10GENIChomozygous990935218
5159591711159591712GA14GENIChomozygous990935219
5159591959159591960CT23GENIChomozygous990935220
5159592241159592242AG24GENIChomozygous990935221
5159592593159592594GA28GENIChomozygous990935222
5159592713159592714CT14GENIChomozygous990935223
5159593011159593012TA21GENIChomozygous990935224
5159593229159593230AG24GENIChomozygous990935225
5159593316159593317AC21GENIChomozygous990935226
5159595521159595522GA14GENIChomozygous990935227
5159598268159598269GA17GENIChomozygous990935228
5159599504159599505TC11GENIChomozygous990935229
5159600471159600472TC11GENIChomozygous990935230
5159601143159601144CT20GENIChomozygous990935231
5159601217159601218AG18GENIChomozygous990935232
5159601274159601275AG22GENIChomozygous990935233
5159602018159602019CT10GENIChomozygous990935234