chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
53028470430284705AACTGGG10GENIChomozygous55270009
53028671130286712GA21GENIChomozygous55270012
53028691330286914AC25GENIChomozygous55270015
53028698430286985TC25GENICpossibly homozygous55270018
53028735130287353AA--16GENIChomozygous55270021
53028743430287435CA2GENIChomozygous55270024
53028851030288511TTC3GENICheterozygous55270027
53028886830288870TT--12GENIChomozygous55270030
53028907430289075AC20GENIChomozygous55270033
53028926030289261CCT3GENICheterozygous55270036
53028931130289312CG20GENIChomozygous55270039
53028970830289709CT24GENICpossibly homozygous55270042
53028984630289847CT16GENIChomozygous55270045
53028992730289928TC20GENIChomozygous55270048
53029059330290594TC1GENIChomozygous55270063
53029062430290625GA3GENIChomozygous55270066
53029066430290665GA1GENIChomozygous55270068