| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200685-6200764 | Common:1; Rare:12 | ||||
| chr12:6341835-6342208 | Common:1; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6383968-6384452 | Common:2; Rare:122 | ||||
| chr12:6452078-6452125 | Common:1; Rare:13 | ||||
| chr12:6470643-6470769 | Common:1; Rare:42 | ||||
| chr12:6493132-6493394 | Common:7; Rare:81 | ||||
| chr12:6493763-6494126 | Common:2; Rare:107 | ||||
| chr12:6534264-6534582 | Common:5; Rare:131 | ||||
| chr12:6534681-6534860 | Common:3; Rare:74 | ||||
| chr12:6536491-6536793 | Rare:98 | ||||
| chr12:6568246-6568388 | Rare:54 | ||||
| chr12:6606272-6606579 | Common:4; Rare:130 | ||||
| chr12:6688879-6689335 | Rare:136 | ||||
| chr12:6689350-6689750 | Common:3; Rare:106 | ||||
| chr12:6723970-6724172 | Rare:53 |