chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115475057115475058TC11GENICheterozygous112815706
4115476171115476172TC22GENIChomozygous112815708
4115476442115476443GA24GENIChomozygous112815710
4115476474115476475TA25GENIChomozygous112815712
4115476501115476502GA19GENIChomozygous112815714
4115476722115476723AG21GENIChomozygous112815716
4115477341115477342AG19GENIChomozygous112815718
4115478351115478352TG13GENICheterozygous112815720
4115478489115478490AG17GENIChomozygous112815722
4115479171115479172TC31GENIChomozygous112815724
4115480465115480466AG15GENIChomozygous112815726
4115481701115481702CT11GENIChomozygous112815728
4115481865115481866GC3GENICheterozygous126099927
4115481866115481867CG6GENIChomozygous112815730
4115481873115481874GA7GENIChomozygous112815732
4115483110115483111TC17GENIChomozygous112815734
4115483945115483946TC19GENIChomozygous112815736
4115484515115484516GA25GENIChomozygous112815738