chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159420352159420353GC24GENIChomozygous75151804
1159422210159422211CA28GENIChomozygous74574179
1159422527159422528AC19GENIChomozygous75151807
1159422740159422741GA22GENIChomozygous74574182
1159430813159430814CT19GENIChomozygous75151808
1159431198159431199CT22GENIChomozygous75151809
1159433719159433720CA31GENIChomozygous74574192
1159435175159435176CT27GENIChomozygous75151810
1159435958159435959GC30GENIChomozygous74574201
1159437697159437698GA14GENIChomozygous75151811
1159438201159438202TC4GENICheterozygous74574210
1159441189159441190CT29GENICpossibly homozygous75151813
1159442951159442952TC28GENIChomozygous74574231
1159443172159443173AG23GENIChomozygous74574234
1159443680159443681GT29GENIChomozygous74574237
1159445084159445085AG22GENIChomozygous75151814
1159446245159446246CT21GENIChomozygous75151815
1159446809159446810AG25GENIChomozygous74574252
1159446896159446897AG29GENIChomozygous74574255
1159447782159447783CT42GENIChomozygous75151816
1159451511159451512TG26GENIChomozygous74574259
1159453232159453233CT33GENIChomozygous75151817
1159454204159454205AC4GENIChomozygous75151818
1159459794159459795TC23GENIChomozygous74574265
1159463360159463361AG38GENIChomozygous74574277
1159463548159463549TC22GENIChomozygous74574280
1159464174159464175AG32GENIChomozygous74574283
1159464230159464231AG30GENIChomozygous74574285
1159464347159464348TC22GENIChomozygous75151819
1159464811159464812AG38GENIChomozygous74574291
1159465190159465191TC22GENIChomozygous74574297
1159465201159465202GA23GENIChomozygous74574299
1159467543159467544CT21GENIChomozygous74574305