| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:206213058-206213636 | Common:2; Rare:199 | ||||
| chr2:206213643-206213781 | Rare:30 | ||||
| chr2:206274520-206274746 | Common:1; Rare:64 | ||||
| chr2:206274840-206275200 | Common:2; Rare:96 | ||||
| chr2:206443402-206443614 | Common:1; Rare:84 | ||||
| chr2:206443874-206444367 | Common:2; Rare:168 | ||||
| chr2:206765261-206765395 | Common:1; Rare:45 | ||||
| chr2:206765527-206765673 | Common:2; Rare:43; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207166137-207166446 | Common:4; Rare:135 | ||||
| chr2:207166816-207167054 | Common:3; Rare:99 | ||||
| chr2:207529631-207530246 | Common:3; Rare:167 | ||||
| chr2:207624963-207625188 | Common:2; Rare:59 | ||||
| chr2:207625390-207625619 | Rare:59 | ||||
| chr2:207711259-207711657 | Common:1; Rare:113 | ||||
| chr2:207769871-207770196 | Common:1; Rare:102 |