chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137886059778860598TC22GENIChomozygous114402118
137886083278860833TA19GENIChomozygous114929469
137886094978860950TA13GENIChomozygous114402120
137886124878861249GC21GENIChomozygous114402122
137886321578863216CT27GENICpossibly homozygous114402124
137886410578864106AG30GENIChomozygous114402128
137886416978864170CT22GENIChomozygous114402130
137886492678864927CT12GENIChomozygous114929473
137886655278866553CT27GENIChomozygous114929475
137886723378867234TG20GENIChomozygous114402132
137886728978867290TC7GENIChomozygous114402134
137887178078871781TC19GENIChomozygous114402136
137887234478872345CT18GENIChomozygous114929477
137887239678872397AT19GENIChomozygous114929479
137887258278872583AT19GENIChomozygous114402140
137887258878872589AC20GENIChomozygous114402142
137887328778873288AG26GENIChomozygous114402144
137887517178875172CA21GENIChomozygous114402152
137887537378875374GA16GENIChomozygous114929481
137887700678877007AG19GENIChomozygous114402154
137887756078877561AG12GENIChomozygous114402156
137887911678879117AG8GENIChomozygous114402160
137888002478880025GT19GENIChomozygous114402162
137888074378880744GA25GENIChomozygous114402164
137888176878881769GA18GENIChomozygous114929483
137888416678884167CT18GENIChomozygous114402166