chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103856179638561797CT22GENIChomozygous52042986
103856193738561938AG23GENIChomozygous51853062
103856233238562333AC24GENIChomozygous51853065
103856237438562375CG24GENIChomozygous51853068
103856247838562479CA20GENIChomozygous51853071
103856272138562725GTGC----29GENICpossibly homozygous51985044
103856282538562826TC29GENIChomozygous51853079
103856290738562908TTTTTA11GENIChomozygous51853082
103856298038562981TC18GENICpossibly homozygous51853084
103856307238563073CT11GENIChomozygous52042988
103856318138563182AG21GENIChomozygous51853087
103856323638563237AC29GENIChomozygous51853090
103856332638563327GA32GENIChomozygous52042990
103856344238563443AG32GENIChomozygous51853093
103856365538563656CCAG14GENIChomozygous52042992
103856382938563830CT23GENIChomozygous51853096
103856391038563912AA--25GENICpossibly homozygous51853100
103856421238564213AAG24GENICpossibly homozygous52042994
103856424338564244CG21GENIChomozygous52043000
103856438538564386AG25GENIChomozygous51853109
103856466438564665GA36GENIChomozygous52043002
103856470538564706TTC45GENIChomozygous51853112