chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135024407150244072CA25GENICpossibly homozygous126066009
135024425350244254AG15GENIChomozygous126066010
135024820950248210AG16GENIChomozygous126066011
135024954550249546CA5GENIChomozygous126066012
135025325150253252GA14GENIChomozygous126066013
135025327250253273CT13GENIChomozygous126066014
135025336950253370GT19GENIChomozygous126066015
135025348250253483CT14GENIChomozygous126066016
135025357650253577CT8GENIChomozygous126066017
135025396350253964GA11GENIChomozygous126066018
135025465150254652CA22GENIChomozygous126066019
135025562650255627AG17GENIChomozygous126066020
135025584550255846TC24GENIChomozygous126066021
135025607950256080GA16GENIChomozygous126066022
135025702550257026GA17GENIChomozygous126066023
135025777250257773GA19GENIChomozygous126066024
135025853150258532TC23GENIChomozygous126066025
135025913650259137AG6GENIChomozygous126066026
135025922750259228CT25GENIChomozygous126066027
135025931550259316TC13GENIChomozygous126066028
135025953050259531TC27GENIChomozygous126066029
135025975650259757CT17GENIChomozygous126066030
135025979550259796AC20GENIChomozygous126066031
135025987250259873TC25GENIChomozygous126066032
135026135050261351AG16GENIChomozygous126066033