chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4159434863159434863ATATACATACATATGTACATATACATACATATATACATATACATACATATACATACATATGTACATATACATACATATAC30GENIChomozygous128097591
4159435447159435448AC10GENIChomozygous133480266
4159437517159437518T22GENIChomozygous128097592
4159447914159447914T5GENIChomozygous128097595
4159447932159447932C7GENIChomozygous128097596
4159447946159447947T7GENIChomozygous128097597
4159447960159447960G11GENIChomozygous128097598
4159447969159447970G11GENIChomozygous128097599
4159447991159447991G12GENIChomozygous128097600
4159453554159453556AA9GENIChomozygous128097601
4159453560159453561T9GENIChomozygous128097602
4159453565159453566T9GENIChomozygous128097603
4159453585159453586A14GENIChomozygous128097604
4159453610159453611C13GENIChomozygous128097605
4159453614159453615A13GENIChomozygous128097606
4159453619159453620T13GENIChomozygous128097607
4159453636159453636A12GENIChomozygous128097608
4159453643159453643T12GENIChomozygous128097609
4159453680159453680CA8GENIChomozygous128097610
4159453689159453690A8GENIChomozygous128097611
4159453691159453692A3GENIChomozygous134685295
4159453695159453696A2GENIChomozygous134685296
4159453707159453708A2GENIChomozygous134685297
4159453709159453710A2GENIChomozygous134685298
4159453711159453713CA2GENIChomozygous134685299
4159453665159453666GA11GENIChomozygous112912826
4159455666159455667TG18GENIChomozygous112912828