chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4152861529152861530TC19GENIChomozygous112888818
4152862775152862776AG11GENIChomozygous126026222
4152863082152863083GA7GENICheterozygous126026223
4152863699152863700TC28GENIChomozygous112888819
4152863885152863886TC22GENIChomozygous112888820
4152864914152864915TC22GENIChomozygous112888821
4152865778152865779GA25GENIChomozygous112888823
4152866823152866824GA4GENIChomozygous112888825
4152867392152867393TC17GENIChomozygous112888827
4152868818152868819TC5GENIChomozygous112888829
4152869620152869621TC13GENIChomozygous112888831
4152870093152870094AG8GENIChomozygous112888832
4152871140152871141GA11GENIChomozygous112888834
4152872133152872134TG11GENIChomozygous112888836
4152872281152872282TC4GENICheterozygous126150532
4152874076152874077GT14GENIChomozygous112888838
4152874377152874378CA29GENIChomozygous112888839
4152876056152876057TC17GENICpossibly homozygous112888840
4152876493152876494CA13GENIChomozygous112888842
4152878068152878069CG5GENICheterozygous126026224
4152878658152878659CT8GENIChomozygous112888845
4152879646152879647CA15GENIChomozygous112888846
4152881988152881989CT11GENIChomozygous112888848
4152886132152886133TC23GENIChomozygous112888849
4152887527152887528TG11GENIChomozygous112888850
4152887679152887680AG23GENIChomozygous112888851
4152888189152888190GC17GENIChomozygous112888852
4152890102152890103AG11GENIChomozygous112888855
4152890221152890222CA15GENIChomozygous112888856
4152890992152890993CT6GENIChomozygous112888858
4152891941152891942GA18GENIChomozygous112888861