| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:113422110-113422424 | Common:2; Rare:66 | ||||
| chr12:113966274-113966530 | Common:17; Rare:166 | ||||
| chr12:114682724-114683200 | Common:1; Rare:160; Clinvar:5; Clinvar (benign):2 | ||||
| chr12:114683859-114684732 | Common:12; Rare:427; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:116276290-116277040 | Common:9; Rare:415 | ||||
| chr12:116277118-116277518 | Common:3; Rare:126 | ||||
| chr12:116277532-116277873 | Common:2; Rare:227 | ||||
| chr12:116737956-116738356 | Common:10; Rare:261 | ||||
| chr12:116910897-116911060 | Rare:54 | ||||
| chr12:117099323-117099571 | Common:2; Rare:146 | ||||
| chr12:118052450-118052840 | Common:8; Rare:96 | ||||
| chr12:118061037-118061474 | Common:9; Rare:165 | ||||
| chr12:118103820-118104110 | Common:2; Rare:135 | ||||
| chr12:118135917-118136220 | Common:4; Rare:172 | ||||
| chr12:118372754-118373306 | Common:5; Rare:266 |