| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:50050620-50050762 | Rare:24 | ||||
| chr12:50050817-50050987 | Rare:39 | ||||
| chr12:50170254-50170544 | Rare:39 | ||||
| chr12:50186434-50186532 | Common:1; Rare:16 | ||||
| chr12:50186822-50186886 | Rare:12 | ||||
| chr12:50187587-50187795 | Common:1; Rare:29 | ||||
| chr12:50211905-50212054 | Common:2; Rare:19 | ||||
| chr12:50247095-50247401 | Common:2; Rare:46 | ||||
| chr12:50342175-50342238 | Rare:5 | ||||
| chr12:50505624-50505749 | Common:1; Rare:37 | ||||
| chr12:50506129-50506259 | Rare:22 | ||||
| chr12:50530090-50530191 | Common:1; Rare:29 | ||||
| chr12:50546065-50546215 | Common:1; Rare:22 | ||||
| chr12:50546503-50546719 | Rare:27 | ||||
| chr12:50589542-50589707 | Rare:31 |