chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155593660155593661G-14GENIChomozygous56993552
4155593743155593744G-5GENIChomozygous56993553
4155593749155593750G-7GENIChomozygous56993554
4155594736155594737CCTTGG13GENIChomozygous56993565
4155597318155597319TTTCATG10GENIChomozygous56993583
4155599643155599644AAGG12GENICheterozygous56993595
4155599646155599647CG18GENIChomozygous56993597
4155601026155601027GGA1GENIChomozygous56993620
4155603387155603388AT29GENIChomozygous56993635
4155613879155613880CT11GENICheterozygous56993674
4155613891155613892TC11GENICheterozygous56993675
4155613922155613923AG10GENICheterozygous56993676
4155619170155619171GA26GENIChomozygous56993695
4155624988155624989TC25GENIChomozygous56993719
4155613896155613897AG12GENICheterozygous57957782
4155648380155648381A-16GENIChomozygous56993721
4155648856155648860TTTG----22GENICheterozygous57526418
4155649172155649173GA15GENIChomozygous57957785
4155653885155653886TG4GENICheterozygous56993724
4155656069155656072GGG---3GENICheterozygous56993730
4155656090155656091TA6GENICheterozygous56993731