| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:8033463-8033606 | Rare:39 | ||||
| chr12:8227579-8227691 | Rare:29 | ||||
| chr12:8650253-8650527 | Common:3; Rare:57; Clinvar (benign):2 | ||||
| chr12:8697222-8697316 | Common:1; Rare:17 | ||||
| chr12:8697489-8697777 | Rare:90 | ||||
| chr12:8697837-8698269 | Common:5; Rare:153 | ||||
| chr12:8868181-8868278 | Common:2; Rare:29; Clinvar (benign):2 | ||||
| chr12:8914155-8914230 | Rare:16 | ||||
| chr12:8914310-8914764 | Common:7; Rare:133 | ||||
| chr12:8915173-8915378 | Rare:50 | ||||
| chr12:8949384-8950141 | Common:4; Rare:162 | ||||
| chr12:9115854-9116023 | Common:3; Rare:40 | ||||
| chr12:9116114-9116417 | Rare:54 | ||||
| chr12:9664702-9665168 | Common:3; Rare:81 | ||||
| chr12:9760898-9761077 | Rare:23 |