chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159420352159420353GC26GENIChomozygous75151804
1159421743159421744GA9GENICpossibly homozygous75151806
1159422527159422528AC24GENIChomozygous75151807
1159422740159422741GA38GENIChomozygous74574182
1159430813159430814CT24GENIChomozygous75151808
1159431198159431199CT23GENIChomozygous75151809
1159433719159433720CA23GENIChomozygous74574192
1159435175159435176CT24GENIChomozygous75151810
1159435958159435959GC33GENIChomozygous74574201
1159437697159437698GA28GENIChomozygous75151811
1159438201159438202TC13GENIChomozygous74574210
1159438206159438207AG11GENIChomozygous74574213
1159438340159438341GA15GENIChomozygous74574222
1159441189159441190CT25GENIChomozygous75151813
1159442951159442952TC19GENIChomozygous74574231
1159443172159443173AG27GENIChomozygous74574234
1159443680159443681GT25GENIChomozygous74574237
1159445084159445085AG21GENIChomozygous75151814
1159446245159446246CT18GENIChomozygous75151815
1159446809159446810AG28GENIChomozygous74574252
1159446896159446897AG25GENIChomozygous74574255
1159447782159447783CT24GENIChomozygous75151816
1159451511159451512TG21GENIChomozygous74574259
1159453232159453233CT22GENIChomozygous75151817
1159454204159454205AC4GENIChomozygous75151818
1159459794159459795TC19GENIChomozygous74574265
1159463360159463361AG34GENIChomozygous74574277
1159463548159463549TC17GENIChomozygous74574280
1159464174159464175AG22GENIChomozygous74574283
1159464230159464231AG15GENIChomozygous74574285
1159464347159464348TC23GENIChomozygous75151819
1159464811159464812AG29GENIChomozygous74574291
1159465190159465191TC25GENIChomozygous74574297
1159465201159465202GA29GENIChomozygous74574299
1159467543159467544CT14GENIChomozygous74574305