chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105590198755901988CT51GENIChomozygous116935061
105590252255902523TC17GENIChomozygous118039025
105590284855902849TC20GENIChomozygous116782972
105590322255903223CT40GENIChomozygous116782976
105590335055903351CG40GENIChomozygous116782978
105590360855903609GA40GENIChomozygous116935063
105590386155903862CT33GENIChomozygous116782982
105590410255904103AT44GENIChomozygous116782984
105590456655904567CT47GENICpossibly homozygous116935065
105590484055904841GA38GENIChomozygous116935067
105590507955905080GT22GENIChomozygous116782986
105590548955905490AG40GENICpossibly homozygous116935069
105590563955905640CT41GENIChomozygous116935071
105590608255906083TG30GENIChomozygous116782988
105590699955907000GA37GENIChomozygous116935073
105590833655908337CT35GENIChomozygous116782990
105590958155909582GT36GENIChomozygous116935075
105590989755909898TC46GENIChomozygous116783002
105591315455913155AG1GENIChomozygous126460716
105591382955913830CT20GENIChomozygous118039029
105591389755913898CT41GENIChomozygous117179234
105591555455915555TC43GENIChomozygous116783004
105591704855917049TC49GENIChomozygous116935077
105592315855923159AG56GENIChomozygous116783012
105592423855924239GA48GENIChomozygous116783014
105592468455924685CA56GENIChomozygous116783016
105592659155926592AC54GENICpossibly homozygous116783018
105590315655903156C29GENIChomozygous132692076
105590527155905271TT29GENICpossibly homozygous132692077
105590620055906200A32GENIChomozygous132692078