chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159420352159420353GC26GENIChomozygous75151804
1159421743159421744GA17GENICheterozygous75151806
1159422527159422528AC25GENIChomozygous75151807
1159422740159422741GA37GENIChomozygous74574182
1159430813159430814CT19GENIChomozygous75151808
1159431198159431199CT13GENIChomozygous75151809
1159433719159433720CA26GENIChomozygous74574192
1159435175159435176CT13GENIChomozygous75151810
1159435958159435959GC25GENIChomozygous74574201
1159437697159437698GA29GENIChomozygous75151811
1159438201159438202TC14GENICpossibly homozygous74574210
1159438206159438207AG11GENICpossibly homozygous74574213
1159438340159438341GA7GENIChomozygous74574222
1159441189159441190CT31GENIChomozygous75151813
1159442951159442952TC24GENIChomozygous74574231
1159443172159443173AG30GENIChomozygous74574234
1159443680159443681GT21GENIChomozygous74574237
1159445084159445085AG28GENIChomozygous75151814
1159446245159446246CT15GENIChomozygous75151815
1159446809159446810AG33GENIChomozygous74574252
1159446896159446897AG37GENIChomozygous74574255
1159447782159447783CT28GENIChomozygous75151816
1159451511159451512TG20GENIChomozygous74574259
1159453232159453233CT32GENIChomozygous75151817
1159454204159454205AC8GENIChomozygous75151818
1159459794159459795TC30GENIChomozygous74574265
1159464230159464231AG31GENIChomozygous74574285
1159463360159463361AG24GENIChomozygous74574277
1159463548159463549TC20GENIChomozygous74574280
1159464174159464175AG23GENIChomozygous74574283
1159464347159464348TC30GENIChomozygous75151819
1159464811159464812AG28GENIChomozygous74574291
1159465190159465191TC36GENIChomozygous74574297
1159465201159465202GA36GENIChomozygous74574299
1159467543159467544CT36GENIChomozygous74574305