chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105590198755901988CT16GENIChomozygous116935061
105590284855902849TC8GENIChomozygous116782972
105590322255903223CT19GENIChomozygous116782976
105590335055903351CG8GENIChomozygous116782978
105590360855903609GA27GENIChomozygous116935063
105590386155903862CT21GENIChomozygous116782982
105590410255904103AT20GENIChomozygous116782984
105590456655904567CT12GENIChomozygous116935065
105590484055904841GA11GENIChomozygous116935067
105590507955905080GT9GENIChomozygous116782986
105590548955905490AG19GENIChomozygous116935069
105590563955905640CT24GENIChomozygous116935071
105590608255906083TG14GENIChomozygous116782988
105590699955907000GA13GENIChomozygous116935073
105590833655908337CT23GENIChomozygous116782990
105590958155909582GT22GENIChomozygous116935075
105590989755909898TC16GENIChomozygous116783002
105591555455915555TC32GENIChomozygous116783004
105591704855917049TC20GENIChomozygous116935077
105592315855923159AG15GENIChomozygous116783012
105592423855924239GA15GENIChomozygous116783014
105592659155926592AC27GENIChomozygous116783018