chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191049565010495650ACCTGGCCCAG22GENIChomozygous129583521
191049570110495702G27GENIChomozygous129583522
191049570910495710G28GENIChomozygous129583523
191049571710495718TC29GENIChomozygous110169046
191049572710495728GT30GENIChomozygous110058358
191049573210495733T31GENIChomozygous129583524
191049573810495739TC30GENIChomozygous110169048
191049575110495752GA27GENIChomozygous110169050
191049575610495757G27GENIChomozygous129583525
191049576310495764CA28GENIChomozygous119596328
191049576610495767T27GENIChomozygous129583526
191049577010495771TG28GENIChomozygous109634044
191049577210495773AC28GENIChomozygous109634046
191049579010495791C24GENIChomozygous129583527
191049580510495806A26GENIChomozygous129583528
191049581410495815T25GENIChomozygous129583529
191049582710495828C25GENIChomozygous129583530
191050101510501016GT14GENICpossibly homozygous119656103
191050995810509959GT10GENIChomozygous129632148