chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176311224963112250CT16GENIChomozygous119418341
176311463163114632GA12GENIChomozygous125550015
176311631263116313CT12GENIChomozygous125550019
176311673963116740TC7GENIChomozygous125550020
176311805063118051CA20GENIChomozygous125513972
176311478663114787GC4GENICheterozygous125583671
176311489463114895TC10GENIChomozygous125583673
176311716363117164CT12GENIChomozygous125513969
176311896063118961GA11GENIChomozygous125550021
176311901663119017CT6GENIChomozygous125550022
176311966363119664AT5GENIChomozygous125583675
176312170463121705TG7GENIChomozygous125513974
176312170563121706CG9GENIChomozygous125513975
176312217563122176TC4GENIChomozygous125550023
176312429063124291AG10GENICheterozygous125550024
176312594363125944AT4GENIChomozygous125583677
176312594463125945GC4GENIChomozygous125583679
176312700163127002TC4GENIChomozygous125583681
176312723363127234CT16GENICheterozygous125550026
176312732763127328AT22GENIChomozygous125550027
176313921863139219GC8GENIChomozygous125513977
176313932563139326CT10GENIChomozygous125513978
176313932963139330GC14GENIChomozygous125550028
176313937463139375CT26GENIChomozygous125513979
176313965363139654AG17GENIChomozygous125513980
176314048963140490TA32GENIChomozygous125550029
176314064663140647TA11GENIChomozygous125513982
176314072363140724GA12GENIChomozygous125513984
176314160463141605GA25GENIChomozygous125550030
176314164963141650GA24GENIChomozygous125513985
176314184763141848AG5GENIChomozygous125583683
176314233763142338AG14GENIChomozygous125513986
176314237663142377AG13GENIChomozygous125513987
176314241363142414CA15GENIChomozygous125513988
176314383063143831AC16GENIChomozygous125513990
176314421763144218CT16GENIChomozygous125513991
176314483563144836TC26GENIChomozygous125513992
176314509363145094AG19GENIChomozygous125550031
176314536963145370TC18GENIChomozygous125513993