chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121541169315411694AC9GENIChomozygous50073010
121541210115412102GGA11GENIChomozygous50073014
121541292215412923GA5GENIChomozygous50568465
121541502215415023TC4GENIChomozygous50436158
121541702215417023TC9GENIChomozygous50073016
121541769015417691CG3GENIChomozygous50073020
121541769615417697TC2GENIChomozygous50073022
121541772415417725GGA1GENIChomozygous50073026
121541799015417991TC6GENIChomozygous50436160
121541848815418489TTA5GENIChomozygous50436162
121541916215419163AC13GENIChomozygous50073036
121541930615419307GA10GENIChomozygous50436164
121542008115420082GA6GENIChomozygous50073038
121542008315420084GA6GENIChomozygous50282106
121542008515420086AG6GENIChomozygous50282107
121542034715420348CT4GENIChomozygous50073040
121542080515420808AGG---9GENIChomozygous50568466
121542082715420828GA9GENIChomozygous50073044
121542094515420946CT9GENIChomozygous50436166
121542103215421033TA7GENIChomozygous50073046
121542103515421036TG6GENIChomozygous50073048
121542104015421041AC6GENIChomozygous50073050
121542104415421045AG7GENIChomozygous50073052
121542104915421050TA10GENIChomozygous50504038
121542105015421051CA10GENIChomozygous50504039
121542105215421053GC10GENIChomozygous50504040
121542105615421057AC11GENIChomozygous50073054
121542106415421065TA10GENIChomozygous50073056
121542114515421146GGCTCGTCTGGACGCTCTCTATCTTGTCT15GENIChomozygous50504041
121542170615421707CT10GENIChomozygous50073058
121542194615421947AC6GENIChomozygous50073060
121542211215422113TC8GENIChomozygous50073062
121542246915422470A-9GENIChomozygous50073066
121542296015422961TC8GENIChomozygous50073068
121542298515422986AG8GENIChomozygous50073070
121542408515424086CT3GENIChomozygous50073074
121542418015424181GA2GENIChomozygous50073076
121542468015424681TG1GENIChomozygous50073078
121542469415424695CT1GENIChomozygous50073080