chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
855228075522808AATCTATATAAAGTGATCATTTCTATATAAAGTGATCATT10INTERGENIChomozygous53928526
855229155522916GGA8INTERGENIChomozygous53297691
855229265522927CCATT9INTERGENIChomozygous53355301
855240475524048GA10INTERGENIChomozygous53297692
855242395524240GA15INTERGENIChomozygous53297693
855242875524288GT5INTERGENIChomozygous53297694
855245085524509GGCC7INTERGENIChomozygous53297695
855245095524510GC7INTERGENIChomozygous53928528
855248115524812AG17INTERGENIChomozygous53297696
855269325526933AG10INTERGENIChomozygous53297697
855269965526997AG6INTERGENIChomozygous53297698
855270305527031GC9INTERGENIChomozygous53297699
855277265527727AT11INTERGENIChomozygous53297700
855278425527843GGA10INTERGENIChomozygous53297701
855279455527946AG13INTERGENIChomozygous53297702
855286605528662TT--25GENIChomozygous53297703
855286625528663TA25GENIChomozygous53928531
855288015528802AG18GENIChomozygous53297704
855288815528882GT25GENIChomozygous53297705
855292115529212GC38GENIChomozygous53297706
855293745529375AG14GENIChomozygous53297707
855295495529550GGT10GENIChomozygous53297708
855298815529882CT17GENIChomozygous53297709
855299025529903AG18GENIChomozygous53297710
855301605530161GA11GENIChomozygous53297711
855302665530267CT11GENIChomozygous53297712
855303315530332GA6GENIChomozygous53297713
855311095531110AAT18GENIChomozygous53297714
855314795531480AT11GENIChomozygous53297715
855317135531714TC13GENIChomozygous52503232
855319265531927TC22GENIChomozygous52503234
855319545531955TC16GENIChomozygous53297716
855323745532375TC18GENIChomozygous53297717
855324395532440TG17GENIChomozygous53297718
855326845532685CA20GENIChomozygous53297719
855327605532761A-18GENIChomozygous53297720
855327925532793GA15GENIChomozygous52503236