chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115473973115473974GA26GENIChomozygous112815704
4115475057115475058TC9GENICheterozygous112815706
4115475058115475059TC9GENICheterozygous131850850
4115476171115476172TC25GENIChomozygous112815708
4115476442115476443GA21GENIChomozygous112815710
4115476474115476475TA22GENIChomozygous112815712
4115476501115476502GA24GENIChomozygous112815714
4115476722115476723AG18GENIChomozygous112815716
4115477341115477342AG21GENIChomozygous112815718
4115478351115478352TG29GENIChomozygous112815720
4115478489115478490AG19GENIChomozygous112815722
4115479171115479172TC26GENIChomozygous112815724
4115480465115480466AG25GENIChomozygous112815726
4115481701115481702CT19GENIChomozygous112815728
4115481866115481867CG22GENIChomozygous112815730
4115481873115481874GA20GENIChomozygous112815732
4115482177115482177T13GENIChomozygous128070926
4115482907115482907CAAGA7GENIChomozygous128070927
4115483110115483111TC19GENIChomozygous112815734
4115483945115483946TC29GENIChomozygous112815736
4115484515115484516GA18GENIChomozygous112815738