| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112409470-112409654 | Rare:123 | ||||
| chr12:112418667-112419011 | Common:1; Rare:101; Clinvar:4; Clinvar (benign):1 | ||||
| chr12:112906804-112907018 | Common:1; Rare:61 | ||||
| chr12:112938250-112938551 | Common:9; Rare:169 | ||||
| chr12:112978230-112978610 | Common:2; Rare:108 | ||||
| chr12:113135638-113136009 | Common:4; Rare:153 | ||||
| chr12:113152740-113153120 | Common:3; Rare:132 | ||||
| chr12:113153134-113153540 | Rare:233 | ||||
| chr12:113184708-113185156 | Common:5; Rare:235 | ||||
| chr12:113185253-113185843 | Common:30; Rare:635 | ||||
| chr12:113185991-113186611 | Common:1; Rare:203 | ||||
| chr12:113220976-113221607 | Common:11; Rare:411 | ||||
| chr12:113221664-113222536 | Common:5; Rare:208 | ||||
| chr12:113335016-113335275 | Rare:199 | ||||
| chr12:113358332-113358694 | Common:7; Rare:354 |