| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113057190-113057590 | Common:1; Rare:144 | ||||
| chr12:113149618-113149743 | Rare:25 | ||||
| chr12:113184891-113185087 | Common:1; Rare:54 | ||||
| chr12:113185411-113185794 | Common:9; Rare:141 | ||||
| chr12:113220983-113221342 | Common:2; Rare:99 | ||||
| chr12:113221521-113221921 | Common:2; Rare:135 | ||||
| chr12:113335046-113335299 | Rare:78 | ||||
| chr12:113358375-113358651 | Common:2; Rare:109 | ||||
| chr12:113422306-113422424 | Common:1; Rare:31 | ||||
| chr12:113966285-113966561 | Common:9; Rare:91 | ||||
| chr12:116276347-116276789 | Common:7; Rare:281 | ||||
| chr12:116276795-116277195 | Common:3; Rare:202; Clinvar (benign):4 | ||||
| chr12:116277608-116277895 | Common:1; Rare:101 | ||||
| chr12:116738002-116738443 | Common:6; Rare:137 | ||||
| chr12:116880970-116881300 | Common:1; Rare:81 |