chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1263812469263812470CT15GENIChomozygous125327000
1263813162263813163GT20GENIChomozygous125327001
1263813490263813491AT15GENIChomozygous125327002
1263814009263814010GA18GENIChomozygous125327003
1263814049263814050GA21GENIChomozygous125327004
1263814336263814337CT21GENIChomozygous125327005
1263815024263815025GA21GENIChomozygous125327006
1263815347263815348CT17GENIChomozygous125327007
1263815742263815743TC19GENIChomozygous125327008
1263817318263817319CT18GENIChomozygous125327009
1263817741263817742TC20GENIChomozygous125327010
1263818713263818714CT24GENIChomozygous125327011
1263820710263820711AG6GENIChomozygous125410983
1263820811263820812TC23GENIChomozygous125327012
1263820859263820860GA18GENIChomozygous125327013
1263823241263823242GA27GENIChomozygous125327014
1263825763263825764CA13GENIChomozygous125327015
1263826117263826118CT16GENIChomozygous125327016
1263827329263827330CT17GENICpossibly homozygous125327017
1263828500263828501GT16GENIChomozygous125327018
1263830695263830696CT17GENIChomozygous125327019
1263831720263831721GA16GENIChomozygous125327020
1263832811263832812TC25GENIChomozygous125327021
1263835276263835277GA18GENIChomozygous125327022
1263835924263835925CT9GENIChomozygous125327023
1263840397263840398CT12GENIChomozygous125327024
1263843298263843299TA16GENIChomozygous125327025