| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6340295-6340442 | Common:1; Rare:24 | ||||
| chr12:6372494-6372729 | Rare:40 | ||||
| chr12:6373053-6373301 | Rare:51 | ||||
| chr12:6770189-6770485 | Rare:87 | ||||
| chr12:6962559-6962618 | Rare:10 | ||||
| chr12:6963048-6963271 | Common:1; Rare:49 | ||||
| chr12:6963531-6963765 | Common:2; Rare:46 | ||||
| chr12:6974149-6974399 | Rare:69 | ||||
| chr12:8242940-8243239 | Common:8; Rare:84 | ||||
| chr12:9072777-9072993 | Rare:57 | ||||
| chr12:9079757-9079860 | Rare:29 | ||||
| chr12:9093519-9093753 | Common:2; Rare:56; Clinvar (benign):1 | ||||
| chr12:9098644-9098952 | Rare:68 | ||||
| chr12:9240318-9240394 | Common:1; Rare:16 | ||||
| chr12:9283905-9284072 | Common:4; Rare:8 |