chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53028470430284705AACTGGG12GENIChomozygous55270009
53028671130286712GA28GENIChomozygous55270012
53028691330286914AC17GENIChomozygous55270015
53028698430286985TC14GENIChomozygous55270018
53028735130287353AA--19GENIChomozygous55270021
53028743430287435CA15GENIChomozygous55270024
53028851030288511TTC17GENIChomozygous55270027
53028886830288870TT--19GENIChomozygous55270030
53028907430289075AC22GENIChomozygous55270033
53028926030289261CCT16GENICpossibly homozygous55270036
53028931130289312CG29GENIChomozygous55270039
53028970830289709CT35GENIChomozygous55270042
53028984630289847CT20GENIChomozygous55270045
53028992730289928TC26GENIChomozygous55270048
53029004730290048GGGACAGCAGCAGC12GENIChomozygous55270051
53029028230290283AT17GENIChomozygous55270054
53029048330290484CCTG20GENIChomozygous55270057
53029057630290577CA29GENIChomozygous55270060
53029059330290594TC30GENIChomozygous55270063
53029062430290625GA26GENIChomozygous55270066
53029066430290665GA19GENIChomozygous55270068