chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121541169315411694AC28GENIChomozygous50073010
121541199515411996AG23GENIChomozygous50073012
121541210115412102GGA11GENIChomozygous50073014
121541702215417023TC33GENIChomozygous50073016
121541703715417041AGTG----32GENIChomozygous50073018
121541769015417691CG11GENIChomozygous50073020
121541769615417697TC9GENIChomozygous50073022
121541770915417710TA10GENIChomozygous50073024
121541772415417725GGA9GENIChomozygous50073026
121541898215418983TTA8GENIChomozygous50073034
121541916215419163AC23GENIChomozygous50073036
121542008115420082GA30GENIChomozygous50073038
121542008315420084GA30GENIChomozygous50282106
121542008515420086AG30GENIChomozygous50282107
121542034715420348CT23GENIChomozygous50073040
121542081215420813GA20GENIChomozygous50073042
121542082715420828GA20GENIChomozygous50073044
121542103215421033TA15GENIChomozygous50073046
121542103515421036TG16GENIChomozygous50073048
121542104015421041AC15GENIChomozygous50073050
121542104415421045AG13GENIChomozygous50073052
121542105615421057AC18GENIChomozygous50073054
121542106415421065TA19GENIChomozygous50073056
121542114515421146GGCTCGTCTGGACGCTCTCTATCTTGTCT27GENIChomozygous50504041
121542104915421050TA16GENIChomozygous50504038
121542105015421051CA17GENIChomozygous50504039
121542105215421053GC17GENIChomozygous50504040
121542170615421707CT29GENIChomozygous50073058
121542194615421947AC21GENIChomozygous50073060
121542211215422113TC21GENIChomozygous50073062
121542241515422416GA19GENIChomozygous50073064
121542246915422470A-25GENIChomozygous50073066
121542296015422961TC30GENIChomozygous50073068
121542298515422986AG28GENIChomozygous50073070
121542373815423743AACAA-----11GENIChomozygous50533712
121542408515424086CT17GENIChomozygous50073074
121542418015424181GA28GENIChomozygous50073076
121542468015424681TG14GENIChomozygous50073078
121542469415424695CT13GENIChomozygous50073080