chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8115345314115345315GA16GENIChomozygous116987672
8115345502115345503CT22GENIChomozygous116987673
8115346353115346354GA17GENIChomozygous116987674
8115346931115346932AG20GENIChomozygous116666314
8115347221115347222GT28GENIChomozygous116987675
8115347657115347658AG18GENIChomozygous116666330
8115348131115348132CT15GENIChomozygous116987676
8115348628115348628CACCCATGACTGACACCCGGCAC16GENIChomozygous128634402
8115348784115348785TC20GENIChomozygous116666344
8115348807115348808TC16GENIChomozygous116666346
8115351181115351182AG17GENIChomozygous116666350
8115351596115351596T21GENIChomozygous128634405
8115351838115351839AG22GENIChomozygous116987679
8115352068115352069AG17GENIChomozygous116987680
8115351381115351381AC12GENIChomozygous132669764
8115352263115352263A16GENIChomozygous132669765
8115352271115352272TC20GENIChomozygous116987681
8115354161115354162C27GENIChomozygous132669766
8115354441115354442TG11GENIChomozygous116987682
8115354517115354518AG13GENIChomozygous116987683
8115355082115355083CA24GENIChomozygous116987684
8115356431115356432GA20GENIChomozygous116987685
8115357573115357574GA17GENIChomozygous116987686
8115358136115358137TC10GENIChomozygous116666360
8115358322115358323GA20GENIChomozygous116987687