chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
73433498534334986GA17GENIChomozygous116015964
73433556234335563CA9GENIChomozygous116015968
73433607634336077CT14GENIChomozygous116015970
73433655134336552TC16GENIChomozygous116015974
73433661834336619CT12GENIChomozygous116015976
73433662334336624GC13GENIChomozygous116015978
73433707034337071AG10GENIChomozygous116015980
73433717634337177TC14GENIChomozygous116015982
73433719334337194GA18GENIChomozygous116015984
73433731034337311AG11GENIChomozygous116015986
73433732634337327GA14GENIChomozygous116015988
73433736434337365TC28GENIChomozygous116015990
73433843534338436AG9GENIChomozygous116015998
73433844434338445GA7GENIChomozygous116327727
73433877434338775CT7GENIChomozygous116327728
73433979734339798CT17GENIChomozygous116016000
73433981734339818GC16GENIChomozygous116016002
73434179434341795AG17GENIChomozygous116016004
73434233134342332CT8GENIChomozygous116016006
73434390234343903AC21GENIChomozygous116016010
73434451634344517CT8GENIChomozygous116016012
73434458934344590AG18GENIChomozygous116016014
73434462234344623GA28GENIChomozygous116016016
73434544034345441CT7GENIChomozygous116327729
73434544434345445CT8GENIChomozygous116016018
73434623934346240CT9GENIChomozygous116327730
73434625434346255TC10GENIChomozygous116016020
73434665034346651CT16GENIChomozygous116016022
73434778934347790GC24GENIChomozygous116016024
73434878934348790GA17GENIChomozygous116016026
73435037634350377AT9GENICheterozygous126615072
73435040434350405AT5GENICheterozygous115642278
73435052934350530AT11GENICheterozygous126567942
73435062434350625TC21GENICheterozygous116016037
73435085834350859CT23GENIChomozygous116016043
73435155634351557TC16GENIChomozygous116016045
73435323534353236GT11GENIChomozygous116016046
73435608234356083GA16GENIChomozygous116016048
73435027834350279TG9GENICheterozygous116140775