chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121639259816392599TC43GENIChomozygous115270187
121639357116393572TC32GENICheterozygous118246355
121639349116393492TC67GENICheterozygous118246352
121639349716393498TC76GENICheterozygous118246353
121639356216393563TC34GENICheterozygous118246354
121639371816393719AG46GENIChomozygous115270189
121639387516393876TC44GENIChomozygous115270191
121639409016394091CT46GENIChomozygous115270193
121639435116394352TC52GENICpossibly homozygous115270195
121639449516394496TC58GENIChomozygous115270197
121639452316394524AG57GENIChomozygous115270199
121639588916395890AT27GENIChomozygous118246356
121639634216396343AG45GENIChomozygous115270201
121639641416396415TC64GENIChomozygous115270203
121639587516395876CT34GENICpossibly homozygous115421172
121639587716395878CT33GENICpossibly homozygous115421174
121639616316396164AT27GENIChomozygous115364521
121639674416396745TG47GENICheterozygous118246357
121639727716397278TC14GENICheterozygous115421176
121639755316397554TG31GENIChomozygous115270207
121639757916397580AG24GENIChomozygous115505258
121639762316397624TC30GENICpossibly homozygous115364522
121639811916398120AG34GENIChomozygous115270209
121639826616398267GA54GENIChomozygous115270211
121639829916398300AG48GENIChomozygous115270213