| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:3753441-3753624 | Common:1; Rare:31 | ||||
| chr12:3873025-3873255 | Common:1; Rare:63 | ||||
| chr12:3873320-3873612 | Common:2; Rare:66 | ||||
| chr12:4273444-4273858 | Rare:108 | ||||
| chr12:4274137-4274200 | Rare:12 | ||||
| chr12:4275727-4275973 | Rare:51 | ||||
| chr12:4320880-4321314 | Common:5; Rare:163 | ||||
| chr12:4321421-4321566 | Rare:29 | ||||
| chr12:4538334-4538946 | Common:3; Rare:151 | ||||
| chr12:4567151-4567325 | Common:1; Rare:36 | ||||
| chr12:4604808-4604993 | Common:4; Rare:67 | ||||
| chr12:4605068-4605135 | Rare:18 | ||||
| chr12:4648546-4649246 | Common:7; Rare:166; Clinvar (benign):2 | ||||
| chr12:4649279-4649399 | Rare:22 | ||||
| chr12:4910789-4910918 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 |