chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
85367878353678784CG14GENIChomozygous116491445
85367879653678797GA12GENIChomozygous116491447
85367880753678808GC15GENIChomozygous116491449
85367881153678812GC15GENIChomozygous116491451
85367882553678826TC13GENIChomozygous116491453
85367883553678836GC14GENIChomozygous116491455
85367885853678859T17GENIChomozygous128591026
85369488453694885G31GENIChomozygous128591029
85369489053694891GT30GENIChomozygous116491475
85369490953694910T31GENIChomozygous128591030
85369491953694920G30GENIChomozygous128591031
85369492153694922T29GENIChomozygous128591032
85369496753694968GT27GENIChomozygous122972208
85369497953694980G26GENIChomozygous128591033
85369499053694990G26GENIChomozygous128591034
85369499253694992A27GENIChomozygous128591035
85369499853694998G27GENIChomozygous128591036
85369503153695032A22GENIChomozygous128591037
85369505453695055G19GENIChomozygous128591038
85369506353695063C18GENIChomozygous128591039
85369513453695135G7GENIChomozygous128591040
85369515353695155CC12GENIChomozygous128591041
85369524553695245C20GENIChomozygous128591042
85369525853695259G21GENIChomozygous128591043
85369543453695435T20GENIChomozygous128591044
85369552153695522A15GENIChomozygous128591045
85369489853694899CA30GENIChomozygous118097927
85369489953694900AC30GENIChomozygous118089941
85369492853694929CG29GENIChomozygous118089942
85369493053694931TC29GENIChomozygous118077198
85369496853694969TG28GENIChomozygous118077199
85369499553694996TG27GENIChomozygous118077200
85370432353704324CT11GENIChomozygous116491537
85370432653704341TTATGTGTAGAGAGT10GENIChomozygous128591054
85370434953704350G8GENIChomozygous128591055
85370437153704372G5GENIChomozygous128591056
85371465153714651T19GENIChomozygous128591060
85374030653740306AG17GENIChomozygous128591070