chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2111835770111835771TC37GENIChomozygous503135147
2111835791111835792GT31GENIChomozygous503135148
2111835826111835827AAC26GENIChomozygous683544508
2111835908111835909CT25GENIChomozygous503135149
2111836059111836060TC51GENIChomozygous503135150
2111836218111836219TG59GENIChomozygous503135151
2111836860111836861TA34GENIChomozygous503135152
2111837033111837034CT53GENIChomozygous503135153
2111837055111837056TC55GENICpossibly homozygous503135154
2111837056111837057CT55GENICpossibly homozygous503135155
2111837531111837532AC48GENICpossibly homozygous503135156
2111837554111837555TC49GENIChomozygous503135157
2111837855111837856GA45GENIChomozygous503135158
2111838008111838009TG46GENIChomozygous503135159
2111838338111838339TC20GENIChomozygous503135160
2111838463111838464TC21GENIChomozygous503135161
2111838660111838661CA17GENICpossibly homozygous503135162
2111839273111839274GT12GENIChomozygous504882583
2111839692111839693TC14GENIChomozygous503135163
2111839973111839974CT17GENIChomozygous503135164
2111840740111840741TC30GENIChomozygous503135165
2111841130111841131CT14GENIChomozygous503135166
2111841151111841152TG14GENIChomozygous503135167
2111841673111841674GA8GENICpossibly homozygous503135168
2111841706111841707TC17GENICpossibly homozygous503135169
2111841936111841937CT51GENICpossibly homozygous503135170
2111842216111842217CA60GENICpossibly homozygous503135171