chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
860158136015814CCTA15GENIChomozygous52505458
860181676018168AT2GENICheterozygous52505465
860185696018570TC18GENICheterozygous52505467
860197636019765AA--4GENIChomozygous52505469
860201326020133T-6GENICheterozygous52505473
860202156020216AC6GENIChomozygous52505475
860203886020389TG16GENIChomozygous52505477
860213316021333AG--14GENIChomozygous52505479
860215616021562GC19GENICheterozygous52505481
860217686021769TC22GENIChomozygous52505483
860235036023504GA20GENIChomozygous52505485
860238456023849CACA----11GENICpossibly homozygous52505487
860245436024544AG9GENICheterozygous52505489
860249186024919AAC1GENIChomozygous52505495
860249196024920AAAAAAAAAC1GENIChomozygous52505496
860252766025277TC13GENICheterozygous52505498
860260706026071CT23GENICpossibly homozygous52505500
860282766028277A-2GENIChomozygous52505502
860298946029895CT24GENICheterozygous52505506
860300666030067TC20GENICpossibly homozygous52505508
860307336030747TGCTAGAATTATAG--------------2GENIChomozygous52505510
860308736030874GA24GENIChomozygous52505512
860320726032073CA22GENIChomozygous52505514
860326366032637GA27GENICheterozygous52505516
860331146033115GA30GENICpossibly homozygous52505518