chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104532230245322303GA15GENIChomozygous117078078
104532360245323603GA8GENIChomozygous117078079
104532398145323982CA26GENIChomozygous117078080
104532401545324016CA27GENIChomozygous117078081
104532449445324495CT25GENIChomozygous117078082
104532492845324929GA23GENIChomozygous117078083
104532531745325318CT20GENIChomozygous117078084
104532572345325724TG13GENIChomozygous117103776
104532573945325740TC19GENIChomozygous117103778
104532686545326866AG13GENIChomozygous117078085
104532732645327327TG18GENIChomozygous117078086
104532738345327384AG15GENIChomozygous117078087
104532765445327655GA16GENIChomozygous117078088
104532801845328019AT19GENIChomozygous117078089
104532834345328344CT18GENIChomozygous117078090
104532835845328359AG12GENIChomozygous117078091
104532847545328476AG16GENIChomozygous117078092
104532866445328665TC25GENIChomozygous117078093
104532878445328785GA12GENIChomozygous117078094
104532901145329012GA15GENIChomozygous117078095
104532918945329190GA22GENIChomozygous117078096
104532934145329342CT17GENIChomozygous117078097
104533052945330530GA16GENIChomozygous117078098
104533053045330531GA16GENIChomozygous117078099
104533077545330776GA9GENIChomozygous117078100
104533094545330946CT13GENIChomozygous117078101
104533134645331347CT23GENIChomozygous117078102
104533182645331827CA9GENIChomozygous117078103
104533203245332033CT11GENIChomozygous116583387
104533204645332047CT9GENIChomozygous117078104
104533254245332543TC23GENIChomozygous116583389
104533338545333386AG25GENIChomozygous116583393
104533353845333539GA17GENIChomozygous117078105
104533494645334947GC12GENIChomozygous117078106