chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117003580870035809TC48GENIChomozygous115897429
117003635770036358TC28GENIChomozygous115897431
117003702570037026GA30GENIChomozygous115897433
117003757770037578CT38GENIChomozygous115897435
117003862370038624GA32GENIChomozygous116160875
117003901670039017AC10GENIChomozygous115897437
117003926170039262TC43GENIChomozygous116160877
117003933370039334AG34GENIChomozygous116160879
117003989270039893AG30GENIChomozygous116160881
117004017670040177GA29GENIChomozygous115897441
117004033270040333GA24GENIChomozygous116160883
117004034070040341GA24GENIChomozygous116160885
117004064270040643TC32GENIChomozygous116160887
117004086070040861CT30GENIChomozygous116160889
117004103170041032TA30GENIChomozygous116160891
117004213870042139CG26GENIChomozygous115897447
117004249070042491TC26GENIChomozygous116160897
117004174670041747TG25GENIChomozygous116160893
117004212270042123AG32GENIChomozygous116160895
117004251670042517TC34GENIChomozygous116160899
117004253170042532GA31GENIChomozygous116160901
117004266470042665CT27GENIChomozygous116160903
117004274170042742GA30GENIChomozygous116160905
117004301970043020CT34GENIChomozygous116160907
117004305570043056GA31GENIChomozygous116160909
117004342670043427CG32GENIChomozygous116160911
117004353670043537CT23GENIChomozygous116160913
117004365170043652CG41GENIChomozygous116160915
117004393670043937TC28GENIChomozygous115897449
117004450770044508TC37GENIChomozygous115897451