chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104532230245322303GA11GENIChomozygous117078078
104532360245323603GA23GENIChomozygous117078079
104532398145323982CA28GENIChomozygous117078080
104532401545324016CA34GENIChomozygous117078081
104532449445324495CT24GENIChomozygous117078082
104532492845324929GA20GENIChomozygous117078083
104532531745325318CT30GENIChomozygous117078084
104532573945325740TC12GENIChomozygous117103778
104532425945324260AG35GENIChomozygous117103772
104532426145324262AG35GENIChomozygous117103774
104532572345325724TG9GENIChomozygous117103776
104532686545326866AG30GENIChomozygous117078085
104532732645327327TG24GENIChomozygous117078086
104532738345327384AG20GENIChomozygous117078087
104532765445327655GA19GENIChomozygous117078088
104532801845328019AT19GENIChomozygous117078089
104532834345328344CT21GENIChomozygous117078090
104532835845328359AG19GENIChomozygous117078091
104532847545328476AG26GENIChomozygous117078092
104532866445328665TC32GENIChomozygous117078093
104532878445328785GA29GENIChomozygous117078094
104532901145329012GA35GENIChomozygous117078095
104532918945329190GA27GENIChomozygous117078096
104532934145329342CT35GENIChomozygous117078097
104533052945330530GA22GENIChomozygous117078098
104533053045330531GA22GENIChomozygous117078099
104533077545330776GA14GENIChomozygous117078100
104533094545330946CT22GENIChomozygous117078101
104533134645331347CT26GENIChomozygous117078102
104533182645331827CA29GENIChomozygous117078103
104533203245332033CT39GENIChomozygous116583387
104533204645332047CT33GENIChomozygous117078104
104533254245332543TC22GENIChomozygous116583389
104533338545333386AG39GENIChomozygous116583393
104533353845333539GA18GENIChomozygous117078105
104533494645334947GC22GENIChomozygous117078106