chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5142289462142289463AG22GENICpossibly homozygous137642258
5142290461142290462CT20GENIChomozygous137642259
5142290802142290803GA19GENIChomozygous137642260
5142290954142290955TC18GENIChomozygous137642261
5142291617142291618AG15GENIChomozygous137642262
5142292896142292897TC20GENIChomozygous137642263
5142293004142293005CG15GENIChomozygous137642264
5142294380142294381CT16GENIChomozygous137642265
5142295226142295227TG28GENIChomozygous137642266
5142296720142296721TC21GENIChomozygous137642267
5142296747142296748AG19GENIChomozygous137642268
5142296673142296685GCACTACTCCCA16GENIChomozygous137346944
5142291240142291241T20GENIChomozygous137346942
5142293155142293156C19GENIChomozygous137346943