chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155593660155593661G-14GENIChomozygous56993552
4155593743155593744G-7GENIChomozygous56993553
4155593749155593750G-6GENIChomozygous56993554
4155594736155594737CCTTGG9GENIChomozygous56993565
4155597318155597319TTTCATG2GENIChomozygous56993583
4155603387155603388AT10GENICpossibly homozygous56993635
4155619170155619171GA13GENIChomozygous56993695
4155646605155646606GGCTGCT3GENICheterozygous58287261
4155648380155648381A-13GENICpossibly homozygous56993721
4155666734155666737AAT---8GENICheterozygous58287267
4155686109155686110CT11GENICheterozygous58678568
4155686272155686273GA7GENICheterozygous58678569