chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319746463197465AG17GENIChomozygous116615249
106319929563199296TC20GENIChomozygous116615253
106320170563201706TG9GENIChomozygous116891778
106320210063202101CT8GENIChomozygous116615257
106320212263202123CT11GENIChomozygous116891780
106320343363203434AC19GENIChomozygous116891782
106320740263207403TC11GENIChomozygous116615265
106320944563209446GA15GENIChomozygous116615267
106321088363210884AG19GENIChomozygous116615269
106321177063211771CA16GENIChomozygous116615271
106321347063213471AG21GENIChomozygous116940267
106320841363208414CT14GENIChomozygous116940261
106321255663212557TG18GENIChomozygous116940263
106321424663214247AC6GENIChomozygous116615283
106321530763215308GA12GENIChomozygous116940269
106321844863218449TC12GENIChomozygous116891788
106322053363220534AC22GENIChomozygous116615291
106322265963222660CT15GENIChomozygous116940271
106322320863223209GA17GENIChomozygous116891790
106322627363226274CT18GENIChomozygous116891792
106322853463228535AT17GENIChomozygous116615302
106323056563230566TC21GENIChomozygous116615304
106323109163231092GA17GENIChomozygous116891794
106323130863231309CT14GENIChomozygous116615308
106323314163233142CT17GENIChomozygous116615310