chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1159421355159421356AG28GENIChomozygous74574176
1159422210159422211CA29GENIChomozygous74574179
1159422740159422741GA54GENICpossibly homozygous74574182
1159424447159424448TA3GENIChomozygous75874216
1159430140159430141TC34GENIChomozygous74574187
1159433719159433720CA40GENIChomozygous74574192
1159435342159435343TA30GENIChomozygous74574198
1159435958159435959GC40GENIChomozygous74574201
1159436726159436727TG41GENIChomozygous74574204
1159439798159439799GT4GENIChomozygous75874217
1159439799159439800TG4GENIChomozygous75874218
1159442380159442381AG23GENIChomozygous74574225
1159442951159442952TC39GENICpossibly homozygous74574231
1159443172159443173AG45GENIChomozygous74574234
1159443680159443681GT35GENIChomozygous74574237
1159444068159444069CT25GENIChomozygous74574240
1159434788159434789GT37GENIChomozygous75716872
1159423679159423680GA14GENIChomozygous75716868
1159431022159431023CT26GENIChomozygous75716870
1159445950159445951GA38GENIChomozygous74574246
1159446043159446044CT24GENIChomozygous74574249
1159446809159446810AG54GENIChomozygous74574252
1159446896159446897AG66GENIChomozygous74574255
1159451511159451512TG31GENIChomozygous74574259
1159461839159461840CT48GENIChomozygous75716874
1159462547159462548TG34GENIChomozygous74574271
1159452769159452770CT56GENIChomozygous74574262
1159459794159459795TC23GENIChomozygous74574265
1159460721159460722GA29GENIChomozygous74574268
1159463360159463361AG23GENIChomozygous74574277
1159463548159463549TC40GENICpossibly homozygous74574280
1159464174159464175AG40GENIChomozygous74574283
1159464230159464231AG40GENIChomozygous74574285
1159464811159464812AG43GENICpossibly homozygous74574291
1159464963159464964GA61GENICpossibly homozygous74574294
1159465190159465191TC42GENIChomozygous74574297
1159465201159465202GA38GENIChomozygous74574299
1159467236159467237TC15GENIChomozygous74574302
1159467543159467544CT43GENIChomozygous74574305