| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:203239213-203239251 | Rare:10 | ||||
| chr2:203328122-203328529 | Common:2; Rare:143 | ||||
| chr2:203535208-203535511 | Common:3; Rare:116 | ||||
| chr2:206085771-206085974 | Common:1; Rare:58 | ||||
| chr2:206086127-206086308 | Rare:20 | ||||
| chr2:206159346-206159989 | Common:4; Rare:187; Clinvar (benign):1 | ||||
| chr2:206274548-206274736 | Rare:55 | ||||
| chr2:206274921-206275057 | Common:1; Rare:47 | ||||
| chr2:206765297-206765654 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):5 | ||||
| chr2:207165928-207166122 | Rare:34 | ||||
| chr2:207166166-207166404 | Common:3; Rare:107 | ||||
| chr2:207166839-207166987 | Common:2; Rare:67 | ||||
| chr2:207529611-207530113 | Common:3; Rare:135 | ||||
| chr2:207596644-207596953 | Common:2; Rare:59 | ||||
| chr2:207625176-207625498 | Common:1; Rare:91 |