chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1210477431047744TG30GENIChomozygous115356884
1210505601050561TC16GENIChomozygous115521794
1210551541055155CA32GENIChomozygous115231125
1210551581055159CA33GENIChomozygous115231127
1210551611055162CA34GENIChomozygous115231129
1210551721055173TA38GENIChomozygous115231131
1210551951055196AC42GENIChomozygous115231135
1210552061055207CG39GENIChomozygous115231137
1210783951078396CA32GENIChomozygous115231192
1210784081078409TG25GENIChomozygous115231194
1210784321078433CG17GENIChomozygous115231196
1210941131094114CG31GENIChomozygous115231251
1210941361094137GT32GENIChomozygous115231255
1210941431094144TC32GENIChomozygous115231257
1210941441094145CT32GENIChomozygous115231259
1211425891142590CG18GENIChomozygous115413577
1211425911142592AC18GENIChomozygous115413582
1211443691144370TC19GENIChomozygous115231374
1211887131188714TG18GENICpossibly homozygous115231558
1211888951188896TA17GENIChomozygous115231560
1212077501207751AG35GENIChomozygous115231622
1212092861209287TG22GENICheterozygous115521795
1212277781227779CG25GENIChomozygous115231699
1213079001307901TC24GENIChomozygous115231962
1213156721315673GT24GENIChomozygous115356949
1213157301315731AG33GENIChomozygous115461057
1213157311315732GT31GENIChomozygous115480957
1213218281321829TG27GENIChomozygous115231978
1213236081323609TC32GENIChomozygous115231980
1213236091323610CT32GENIChomozygous115231982
1213238281323829TG24GENIChomozygous115231984
1213259891325990CA35GENIChomozygous115231986
1213260291326030CG32GENIChomozygous115231988
1213261951326196CT30GENIChomozygous115231990
1213271991327200GA28GENIChomozygous115231992
1213272021327203AG29GENIChomozygous115231994