chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53028470430284705AACTGGG34GENIChomozygous55270009
53028671130286712GA21GENIChomozygous55270012
53028691330286914AC30GENIChomozygous55270015
53028698430286985TC30GENIChomozygous55270018
53028735130287353AA--19GENIChomozygous55270021
53028743430287435CA25GENIChomozygous55270024
53028851030288511TTC12GENIChomozygous55270027
53028886830288870TT--27GENIChomozygous55270030
53028907430289075AC23GENIChomozygous55270033
53028926030289261CCT10GENICpossibly homozygous55270036
53028931130289312CG20GENIChomozygous55270039
53028970830289709CT22GENIChomozygous55270042
53028984630289847CT22GENIChomozygous55270045
53028992730289928TC12GENIChomozygous55270048
53029004730290048GGGACAGCAGCAGC8GENIChomozygous55270051
53029028230290283AT4GENIChomozygous55270054
53029048330290484CCTG2GENIChomozygous55270057
53029057630290577CA6GENIChomozygous55270060
53029059330290594TC6GENIChomozygous55270063
53029062430290625GA4GENIChomozygous55270066
53029066430290665GA8GENIChomozygous55270068