chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
826811862681187GT10GENIChomozygous596902153
826812072681208AT13GENICpossibly homozygous596902154
826814902681491AC22GENICpossibly homozygous596902155
826819802681981TG19GENICpossibly homozygous596902156
826837072683708CT1GENIChomozygous596902157
826838642683865CT14GENIChomozygous596902158
826839712683972TC14GENIChomozygous596902159
826840892684090TG14GENIChomozygous596902160
826850182685019CT10GENIChomozygous596902161
826855252685526AG16GENICpossibly homozygous596902162
826863492686350T-4GENIChomozygous727218154
826864892686490CG2GENIChomozygous596902163
826893082689309TC8GENIChomozygous596902164
826902662690267CT16GENICpossibly homozygous596902165
826905612690562CT5GENIChomozygous596902166
826916292691630TG4GENIChomozygous598335700
826917282691729TA2GENIChomozygous598335701
826924892692490CA5GENICheterozygous598335702
826944932694494CT5GENIChomozygous598335703
826956792695680GA9GENICpossibly homozygous598335704
826970242697025CA25GENIChomozygous598335705
826979702697971TA2GENIChomozygous596902167
826980292698030GT14GENIChomozygous596902168
827015502701551AG20GENICheterozygous596902169
827026552702656GGT6GENIChomozygous727218155
827038482703849AT5GENICheterozygous596902170
827055122705513GA12GENICpossibly homozygous596902171
827079192707920T-2GENIChomozygous727218156
827080192708020A-6GENIChomozygous727218157
827083562708357AG11GENICpossibly homozygous596902172
827108742710875AG21GENICpossibly homozygous596902173