Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:15860455-15860572 | Rare:34 | ||||
chr10:16436776-16437022 | Common:2; Rare:55 | ||||
chr10:16817351-16817744 | Common:4; Rare:142 | ||||
chr10:17228468-17228714 | Common:1; Rare:68 | ||||
chr10:17229101-17229354 | Common:2; Rare:48 | ||||
chr10:17643904-17644241 | Common:2; Rare:102 | ||||
chr10:18651579-18651666 | Common:1; Rare:29 | ||||
chr10:27100432-27100582 | Common:3; Rare:45; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154299-27154427 | Rare:33 | ||||
chr10:27155191-27155429 | Common:7; Rare:105; Clinvar:3; Clinvar (benign):7 | ||||
chr10:28532461-28532847 | Common:5; Rare:148 | ||||
chr10:31031841-31032028 | Common:1; Rare:72 | ||||
chr10:31319022-31319244 | Common:2; Rare:67 | ||||
chr10:31928735-31928913 | Common:3; Rare:69 | ||||
chr10:32958149-32958527 | Common:2; Rare:142 |