chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1116765953116765954GT16GENIChomozygous125398983
1116766146116766147CA19GENIChomozygous125283067
1116766418116766419CT26GENIChomozygous125283068
1116767371116767372CT17GENIChomozygous125283069
1116767682116767683CG14GENICheterozygous125283071
1116767757116767758AG10GENIChomozygous125283072
1116767844116767845AC12GENIChomozygous125398985
1116767858116767859TC19GENICheterozygous125283074
1116767859116767860GA19GENICheterozygous125283075
1116768162116768163TC20GENIChomozygous125283076
1116768548116768549GC15GENIChomozygous125283077
1116769940116769941GA10GENIChomozygous125283078
1116770435116770436GA14GENIChomozygous125283079
1116771371116771372AT20GENIChomozygous125283080
1116772766116772767CT11GENIChomozygous125365786
1116773186116773187CG7GENIChomozygous125365787
1116773456116773457CT26GENIChomozygous125283082
1116773634116773635AG21GENIChomozygous125283083
1116773844116773845TC15GENIChomozygous125283084
1116774925116774926CT13GENIChomozygous125283085
1116775006116775007TC18GENIChomozygous125283086
1116775595116775596GC23GENIChomozygous125283088
1116775963116775964CA17GENIChomozygous125283089
1116776171116776172TC8GENIChomozygous125283090
1116777351116777352CA5GENIChomozygous125365788
1116778315116778316AG15GENIChomozygous125283091
1116779508116779509AC19GENIChomozygous125283093
1116774504116774505AC26GENIChomozygous108192167
1116779078116779079AC17GENIChomozygous108192168