| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:111597387-111597561 | Rare:31 | ||||
| chr12:111597700-111598190 | Rare:254 | ||||
| chr12:111598441-111598609 | Rare:83 | ||||
| chr12:111599060-111599835 | Common:16; Rare:578; Clinvar (benign):3 | ||||
| chr12:111685846-111686245 | Rare:316 | ||||
| chr12:111841816-111842521 | Common:14; Rare:437 | ||||
| chr12:111842596-111843374 | Common:6; Rare:443 | ||||
| chr12:112005940-112006240 | Common:7; Rare:66 | ||||
| chr12:112012594-112012994 | Common:3; Rare:129 | ||||
| chr12:112012993-112013626 | Common:3; Rare:563 | ||||
| chr12:112013770-112014408 | Common:1; Rare:180 | ||||
| chr12:112108472-112109011 | Common:7; Rare:316 | ||||
| chr12:112125295-112125648 | Rare:150 | ||||
| chr12:112382287-112382558 | Common:3; Rare:160 | ||||
| chr12:112409124-112409337 | Common:3; Rare:103 |