chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
81745730617457307CT32GENIChomozygous116753832
81746271817462719TC8GENIChomozygous116753844
81746406517464066AC24GENICheterozygous116753846
81746408917464090TC33GENICheterozygous116753848
81746413817464139CT53GENICheterozygous116436391
81746417017464171TA45GENICheterozygous116436392
81747111017471111AG16GENIChomozygous116753878
81747129317471294AC21GENIChomozygous117091715
81747309817473099CT11GENIChomozygous116753880
81747667817476679TC16GENIChomozygous117091716
81747954717479548GA12GENIChomozygous116753894
81748202417482025CT15GENIChomozygous116753916
81748218217482183AG20GENIChomozygous116753918
81748340817483409TC23GENIChomozygous117091719
81748386917483870CT21GENIChomozygous117091720
81748695117486952TC19GENIChomozygous116753932
81748912617489127TC6GENIChomozygous116753944
81748963817489639GA22GENIChomozygous117091721
81749157117491572TC26GENIChomozygous116753950
81749271317492714CT21GENIChomozygous117091722
81749892717498928CT19GENIChomozygous116753982
81750101517501016AT27GENIChomozygous116753996
81750458017504581AT35GENICpossibly homozygous116754008
81750937017509371AC21GENIChomozygous117091726
81750965017509651AG20GENICpossibly homozygous117091727
81751036517510366GA18GENIChomozygous116754068
81751037417510375TC16GENIChomozygous116754070
81751239517512396CG21GENIChomozygous117091728
81751249317512494GA11GENIChomozygous117091729
81751540617515407AG13GENIChomozygous116754136
81751863917518640AC14GENIChomozygous117091730
81752284317522844TC18GENIChomozygous117091731