chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159421743159421744GA18GENICheterozygous75151806
1159422740159422741GA39GENIChomozygous74574182
1159430615159430616GA18GENIChomozygous76095142
1159430813159430814CT21GENIChomozygous75151808
1159432652159432653AT30GENIChomozygous76466322
1159433719159433720CA23GENIChomozygous74574192
1159435175159435176CT20GENIChomozygous75151810
1159435958159435959GC26GENIChomozygous74574201
1159438201159438202TC13GENICheterozygous74574210
1159438206159438207AG13GENICheterozygous74574213
1159438340159438341GA6GENIChomozygous74574222
1159441189159441190CT37GENIChomozygous75151813
1159442951159442952TC27GENIChomozygous74574231
1159443172159443173AG33GENIChomozygous74574234
1159443680159443681GT28GENIChomozygous74574237
1159446245159446246CT34GENICpossibly homozygous75151815
1159446809159446810AG43GENIChomozygous74574252
1159446896159446897AG39GENIChomozygous74574255
1159447782159447783CT35GENICpossibly homozygous75151816
1159429733159429734CT18GENIChomozygous75456028
1159432887159432888CG33GENIChomozygous75456029
1159444871159444872GA19GENIChomozygous75456030
1159447507159447508CT27GENIChomozygous75456031
1159451511159451512TG25GENIChomozygous74574259
1159453232159453233CT25GENIChomozygous75151817
1159454204159454205AC3GENIChomozygous75151818
1159459794159459795TC27GENIChomozygous74574265
1159463360159463361AG35GENIChomozygous74574277
1159463548159463549TC21GENIChomozygous74574280
1159464174159464175AG53GENIChomozygous74574283
1159464230159464231AG49GENIChomozygous74574285
1159464347159464348TC53GENIChomozygous75151819
1159464811159464812AG34GENIChomozygous74574291
1159465190159465191TC22GENIChomozygous74574297
1159465201159465202GA23GENIChomozygous74574299
1159466096159466097GA37GENIChomozygous75456034
1159467543159467544CT32GENIChomozygous74574305