Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:68527355-68527746 | Common:3; Rare:120 | ||||
chr10:68720928-68721324 | Common:2; Rare:123 | ||||
chr10:68721469-68721626 | Rare:52 | ||||
chr10:68721688-68721792 | Common:1; Rare:20 | ||||
chr10:68827108-68827225 | Rare:29 | ||||
chr10:68827416-68827561 | Common:1; Rare:60 | ||||
chr10:68900743-68900940 | Common:1; Rare:68 | ||||
chr10:68900942-68901452 | Common:3; Rare:200 | ||||
chr10:68901460-68901558 | Rare:36 | ||||
chr10:68901718-68901772 | Rare:11 | ||||
chr10:68955720-68955894 | Rare:31 | ||||
chr10:68955993-68956770 | Common:4; Rare:213 | ||||
chr10:68988679-68989154 | Common:4; Rare:141; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:68989226-68989308 | Rare:35 | ||||
chr10:68989476-68989573 | Rare:16 |