chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121541169315411694AC44GENIChomozygous50073010
121541199515411996AG16GENIChomozygous50073012
121541210115412102GGA19GENIChomozygous50073014
121541702215417023TC28GENIChomozygous50073016
121541703715417041AGTG----24GENIChomozygous50073018
121541769015417691CG18GENIChomozygous50073020
121541769615417697TC18GENIChomozygous50073022
121541770915417710TA13GENIChomozygous50073024
121541772415417725GGA11GENIChomozygous50073026
121541773715417738A-2GENIChomozygous50560589
121541898215418983TTA24GENICpossibly homozygous50073034
121541916215419163AC29GENIChomozygous50073036
121542008115420082GA45GENIChomozygous50073038
121542008315420084GA44GENIChomozygous50282106
121542008515420086AG44GENIChomozygous50282107
121542034715420348CT30GENIChomozygous50073040
121542081215420813GA33GENIChomozygous50073042
121542082715420828GA34GENIChomozygous50073044
121542103215421033TA30GENIChomozygous50073046
121542103515421036TG32GENIChomozygous50073048
121542104015421041AC32GENIChomozygous50073050
121542104415421045AG33GENIChomozygous50073052
121542104915421050TA34GENIChomozygous50504038
121542105015421051CA33GENIChomozygous50504039
121542105215421053GC35GENIChomozygous50504040
121542105615421057AC34GENIChomozygous50073054
121542106415421065TA35GENIChomozygous50073056
121542114515421146GGCTCGTCTGGACGCTCTCTATCTTGTCT37GENIChomozygous50504041
121542170615421707CT27GENIChomozygous50073058
121542194615421947AC62GENIChomozygous50073060
121542211215422113TC41GENIChomozygous50073062
121542241515422416GA34GENIChomozygous50073064
121542246915422470A-38GENIChomozygous50073066
121542296015422961TC46GENIChomozygous50073068
121542298515422986AG44GENIChomozygous50073070
121542373815423743AACAA-----23GENIChomozygous50533712
121542408515424086CT40GENIChomozygous50073074
121542418015424181GA32GENIChomozygous50073076
121542468015424681TG20GENIChomozygous50073078
121542469415424695CT19GENIChomozygous50073080