chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159421743159421744GA13GENICheterozygous75151806
1159422740159422741GA14GENIChomozygous74574182
1159430813159430814CT4GENIChomozygous75151808
1159432652159432653AT15GENIChomozygous76466322
1159433719159433720CA15GENIChomozygous74574192
1159435175159435176CT13GENIChomozygous75151810
1159435958159435959GC5GENIChomozygous74574201
1159438201159438202TC1GENIChomozygous74574210
1159438206159438207AG1GENIChomozygous74574213
1159438340159438341GA6GENIChomozygous74574222
1159430615159430616GA8GENIChomozygous76095142
1159429733159429734CT10GENIChomozygous75456028
1159432887159432888CG16GENIChomozygous75456029
1159441189159441190CT18GENIChomozygous75151813
1159442951159442952TC9GENIChomozygous74574231
1159443172159443173AG15GENIChomozygous74574234
1159443680159443681GT16GENIChomozygous74574237
1159444871159444872GA16GENIChomozygous75456030
1159446245159446246CT14GENIChomozygous75151815
1159446809159446810AG11GENIChomozygous74574252
1159446896159446897AG13GENIChomozygous74574255
1159447507159447508CT8GENIChomozygous75456031
1159447782159447783CT11GENIChomozygous75151816
1159451511159451512TG6GENIChomozygous74574259
1159453232159453233CT18GENIChomozygous75151817
1159454204159454205AC1GENIChomozygous75151818
1159459794159459795TC8GENIChomozygous74574265
1159463360159463361AG11GENIChomozygous74574277
1159463548159463549TC13GENIChomozygous74574280
1159464174159464175AG14GENIChomozygous74574283
1159464230159464231AG18GENIChomozygous74574285
1159464347159464348TC18GENIChomozygous75151819
1159464811159464812AG14GENIChomozygous74574291
1159465190159465191TC15GENIChomozygous74574297
1159465201159465202GA11GENIChomozygous74574299
1159466096159466097GA12GENIChomozygous75456034
1159467543159467544CT9GENIChomozygous74574305