| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121209918-121210215 | Common:5; Rare:104 | ||||
| chr12:121210277-121210398 | Common:1; Rare:40 | ||||
| chr12:121296697-121297017 | Common:3; Rare:98 | ||||
| chr12:121351755-121351989 | Common:1; Rare:40 | ||||
| chr12:121352133-121352815 | Common:10; Rare:220 | ||||
| chr12:121352817-121352854 | Rare:7 | ||||
| chr12:121399805-121400441 | Common:5; Rare:203 | ||||
| chr12:121534635-121534880 | Common:2; Rare:46 | ||||
| chr12:121536166-121536420 | Rare:51 | ||||
| chr12:121536991-121537523 | Common:3; Rare:108 | ||||
| chr12:121537538-121537928 | Common:2; Rare:94 | ||||
| chr12:121579279-121579401 | Rare:19 | ||||
| chr12:121579597-121579714 | Rare:25 | ||||
| chr12:121626292-121626690 | Common:2; Rare:152 | ||||
| chr12:121626733-121626935 | Common:5; Rare:117; Clinvar:6; Clinvar (benign):2 |