| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:174487008-174487385 | Common:2; Rare:91 | ||||
| chr2:174597732-174598052 | Rare:34 | ||||
| chr2:174682830-174683020 | Common:1; Rare:77 | ||||
| chr2:175005169-175005354 | Common:2; Rare:65; Clinvar:2 | ||||
| chr2:175168098-175168553 | Common:2; Rare:117 | ||||
| chr2:176002221-176002414 | Common:3; Rare:85 | ||||
| chr2:176129586-176129747 | Rare:88 | ||||
| chr2:176188510-176188668 | Common:1; Rare:59 | ||||
| chr2:177212441-177212821 | Common:4; Rare:152 | ||||
| chr2:177264048-177264172 | Rare:40 | ||||
| chr2:177264563-177264929 | Common:2; Rare:103 | ||||
| chr2:177392659-177393070 | Common:3; Rare:143; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177553031 | Common:4; Rare:86 | ||||
| chr2:177618702-177619018 | Common:7; Rare:88 | ||||
| chr2:178451090-178451408 | Common:6; Rare:99; Clinvar:4; Clinvar (benign):3 |