chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55901708259017083TC24GENIChomozygous113820020
55901737559017376CT36GENIChomozygous113820022
55901747559017476CG34GENICpossibly homozygous113820024
55901856059018561AG6GENIChomozygous113820030
55901935259019353CG49GENICheterozygous113820048
55901944859019449GA55GENICheterozygous113820050
55901945259019453TC55GENICheterozygous113820052
55902085959020860GA3GENIChomozygous113820074
55902164459021645AC40GENIChomozygous113820078
55902282859022829AG34GENIChomozygous113820086
55902336459023365GA29GENIChomozygous113820088
55902227259022273AG23GENICpossibly homozygous114118166
55902569759025698GA6GENIChomozygous114118168