chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115476171115476172TC18GENIChomozygous112815708
4115476442115476443GA24GENIChomozygous112815710
4115476474115476475TA23GENIChomozygous112815712
4115476722115476723AG21GENIChomozygous112815716
4115476766115476767CG23GENIChomozygous134537156
4115478351115478352TG25GENIChomozygous112815720
4115478489115478490AG18GENIChomozygous112815722
4115479171115479172TC34GENIChomozygous112815724
4115479818115479819CG19GENIChomozygous134537157
4115480465115480466AG23GENIChomozygous112815726
4115481701115481702CT20GENIChomozygous112815728
4115481866115481867CG23GENIChomozygous112815730
4115481873115481874GA23GENIChomozygous112815732
4115482907115482907CAAGA13GENIChomozygous128070927
4115483110115483111TC27GENIChomozygous112815734
4115483945115483946TC25GENIChomozygous112815736
4115484127115484128GA25GENIChomozygous134537158