chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1261061195261061196TC8GENIChomozygous108628945
1261061343261061344AG14GENIChomozygous108628946
1261062511261062512TA28GENIChomozygous108628948
1261062607261062608CT24GENIChomozygous108628949
1261063147261063148CT23GENIChomozygous108628950
1261063350261063351CA27GENIChomozygous108628951
1261063577261063578TC27GENIChomozygous108628952
1261064049261064050GC12GENIChomozygous108628954
1261064841261064842TA18GENIChomozygous108628955
1261065122261065123AT19GENIChomozygous108628956
1261065917261065918TC22GENIChomozygous108628957
1261066517261066518TC7GENIChomozygous108628958
1261068056261068057TA24GENIChomozygous108628959
1261068101261068102GA16GENIChomozygous108628960
1261068755261068756GA21GENIChomozygous108628962
1261069194261069195AT22GENIChomozygous108628963
1261069200261069201AT24GENIChomozygous108628964
1261069916261069917AC23GENIChomozygous108628965
1261070246261070247TC14GENIChomozygous108628966