chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1214123032214123033GT39GENIChomozygous788270079
1214123787214123788CT35GENIChomozygous788270080
1214124348214124349AG12GENIChomozygous788270081
1214125087214125088GA24GENIChomozygous788270082
1214126106214126107GA38GENIChomozygous788270083
1214126509214126510CT16GENIChomozygous788270084
1214126561214126562CG7GENIChomozygous788270085
1214127195214127196AG14GENIChomozygous788270086
1214130422214130423CA23GENIChomozygous788270087
1214130767214130768AG19GENIChomozygous788270088
1214131357214131358AG41GENIChomozygous788270089
1214131750214131751CT33GENIChomozygous788270090
1214132380214132381AG35GENIChomozygous788270091
1214133078214133079GA28GENIChomozygous788270092
1214134834214134835GA50GENIChomozygous788270093
1214138857214138858GT23GENIChomozygous788270094
1214140127214140128AC23GENIChomozygous788270095
1214140827214140828GT29GENIChomozygous788270096
1214141343214141344AG19GENIChomozygous788270097
1214142748214142749GA32GENIChomozygous788270098
1214146027214146028TC25GENIChomozygous788270099