chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120520213120520214CT38GENIChomozygous115856574
7120520546120520547CT41GENIChomozygous116303205
7120520607120520608GT34GENIChomozygous116303206
7120521869120521870AG41GENIChomozygous116303207
7120521888120521889TC44GENIChomozygous115856584
7120523233120523234GT15GENIChomozygous116303208
7120523774120523775AG38GENIChomozygous115856594
7120524378120524379TG24GENICheterozygous116303209
7120524806120524807GA19GENIChomozygous116303210
7120525152120525153CT23GENIChomozygous116303211
7120527422120527423TC33GENIChomozygous115856610
7120527557120527558TG38GENIChomozygous116303212
7120528592120528593TC38GENIChomozygous116081686
7120529488120529489GA31GENIChomozygous116303213
7120529677120529678AG37GENIChomozygous115856620
7120530455120530456AG31GENIChomozygous116303214
7120533587120533588TC49GENIChomozygous115856634
7120536664120536665TG40GENIChomozygous115856638
7120538127120538128AG21GENIChomozygous115856644
7120539580120539581CT31GENIChomozygous116303215
7120539954120539955CT23GENIChomozygous116303216
7120540573120540574CT31GENIChomozygous116303217
7120540812120540813TC43GENIChomozygous115856656
7120543162120543163GA40GENIChomozygous116303218
7120543378120543379TC26GENIChomozygous115856664
7120543712120543713GA43GENIChomozygous116303219
7120545354120545355CT42GENIChomozygous116303220
7120546105120546106CA15GENICpossibly homozygous116081716
7120550953120550954CT29GENIChomozygous116303221
7120551148120551149AT31GENIChomozygous116303222
7120552484120552485TC28GENIChomozygous115856684
7120553734120553735CT34GENIChomozygous116303223
7120553739120553740GT35GENIChomozygous115856690
7120558050120558051GT22GENIChomozygous116303224