chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138960818089608181CG13GENIChomozygous114571921
138960831589608316AG9GENIChomozygous114571922
138960921889609219GC9GENIChomozygous114571924
138961063689610637AG11GENIChomozygous114571926
138961274689612747AG14GENIChomozygous114571928
138961291189612912GA12GENIChomozygous114571929
138961328889613289AG11GENIChomozygous114571931
138961386489613865GA10GENIChomozygous114571933
138961386689613867AG9GENIChomozygous114571935
138961411789614118CT7GENIChomozygous114571937
138961435789614358GT14GENIChomozygous114571939
138961504789615048GA12GENIChomozygous114571940
138961632889616329CA11GENIChomozygous114571942
138961633489616335TC10GENIChomozygous114571944
138961748989617490TA4GENIChomozygous114571946
138961843089618431CT11GENIChomozygous114571947
138961846989618470AG10GENIChomozygous114571949
138961882289618823CA12GENIChomozygous114571951
138961916189619162TC9GENIChomozygous114571953
138962091889620919GC4GENIChomozygous114571955
138962095989620960TA3GENIChomozygous114571956
138962161889621619CG6GENIChomozygous114571958
138962168089621681CG5GENICheterozygous114571960
138962176989621770AG5GENIChomozygous114571962
138962216989622170AT8GENIChomozygous114571963
138962308989623090CT6GENIChomozygous114571965
138962310889623109CT7GENIChomozygous114571967