chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115476171115476172TC26GENIChomozygous112815708
4115476442115476443GA23GENIChomozygous112815710
4115476474115476475TA23GENIChomozygous112815712
4115476501115476502GA26GENIChomozygous112815714
4115476722115476723AG26GENIChomozygous112815716
4115477341115477342AG29GENIChomozygous112815718
4115478351115478352TG36GENIChomozygous112815720
4115478489115478490AG27GENIChomozygous112815722
4115479171115479172TC37GENIChomozygous112815724
4115480465115480466AG24GENIChomozygous112815726
4115481701115481702CT17GENIChomozygous112815728
4115481866115481867CG17GENIChomozygous112815730
4115481873115481874GA15GENIChomozygous112815732
4115483110115483111TC30GENIChomozygous112815734
4115483945115483946TC20GENIChomozygous112815736
4115484515115484516GA31GENIChomozygous112815738