chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106319746463197465AG16GENIChomozygous893774155
106319929563199296TC16GENIChomozygous893774156
106320144063201441AG25GENIChomozygous893774157
106320170563201706TG11GENIChomozygous893774158
106320210063202101CT17GENIChomozygous893774159
106320212263202123CT23GENIChomozygous893774160
106320343363203434AC15GENIChomozygous893774161
106320638863206389CA21GENIChomozygous893774162
106320740263207403TC27GENIChomozygous893774163
106320841363208414CT12GENIChomozygous893774164
106320944563209446GA17GENIChomozygous893774165
106321088363210884AG4GENIChomozygous893774166
106321177063211771CA13GENIChomozygous893774167
106321255663212557TG30GENIChomozygous893774168
106321347063213471AG12GENIChomozygous893774169
106321424663214247AC5GENIChomozygous893774170
106321530763215308GA17GENIChomozygous893774171
106321844863218449TC10GENICheterozygous893774172
106322053363220534AC16GENIChomozygous893774173
106322265963222660CT5GENIChomozygous893774174
106322320863223209GA14GENIChomozygous893774175
106322627363226274CT20GENIChomozygous893774176
106322853463228535AT21GENIChomozygous893774177
106323056563230566TC24GENIChomozygous893774178
106323109163231092GA23GENIChomozygous893774179
106323130863231309CT10GENIChomozygous893774180
106323314163233142CT7GENIChomozygous893774181