chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
138353405883534059CT21GENIChomozygous114902111
138353486583534866AT14GENIChomozygous114415242
138354611283546113AG20GENIChomozygous114902113
138354618783546188AG28GENIChomozygous114415260
138354674283546743CT23GENIChomozygous114779620
138354731283547313GT5GENIChomozygous114902115
138354759083547591TC24GENIChomozygous114415264
138354853083548531AC11GENIChomozygous114415270
138354935583549356GT19GENIChomozygous114902117
138355168583551686AG24GENIChomozygous114415286
138355719283557193AG18GENIChomozygous114902119
138355925483559255TC23GENIChomozygous114415326
138355989983559900TC28GENIChomozygous114415336
138356140183561402GA18GENIChomozygous114779626
138356191383561914TG32GENIChomozygous114415350
138356244383562444TC29GENIChomozygous114415352
138356462983564630AG16GENIChomozygous114415370
138356515083565151TC22GENIChomozygous114415374
138357146883571469TC32GENIChomozygous114415396
138357237783572378TG27GENIChomozygous114902121
138357246183572462AT27GENIChomozygous114415404
138357337983573380AG26GENICpossibly homozygous114902123
138357388383573884GA28GENIChomozygous114902125
138357448983574490CT32GENIChomozygous114902127