chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3114721511114721512CA23GENIChomozygous892232778
3114721712114721713GT5GENIChomozygous892232779
3114721796114721797CT20GENIChomozygous892232780
3114721832114721833CG16GENIChomozygous892232781
3114722255114722256CT5GENIChomozygous892232782
3114722517114722518TC21GENIChomozygous892232783
3114722584114722585CT16GENIChomozygous892232784
3114722627114722628CT14GENIChomozygous892232785
3114722944114722945AG14GENIChomozygous892232786
3114723627114723628GC7GENIChomozygous892232787
3114723642114723643TC7GENIChomozygous892232788
3114723649114723650TC7GENIChomozygous892232789
3114723857114723858AG12GENICheterozygous892232790
3114724148114724149TC21GENIChomozygous892232791
3114724249114724250AC12GENIChomozygous892232792
3114724379114724380CG14GENIChomozygous892232793
3114724710114724711CT17GENIChomozygous892232794
3114724794114724795TC25GENICpossibly homozygous892232795
3114724874114724875CT13GENIChomozygous892232796
3114725243114725244CG13GENIChomozygous892232797
3114725495114725496CA17GENIChomozygous892232798
3114725588114725589GA25GENIChomozygous892232799
3114726577114726578GA9GENIChomozygous892232800