| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176129581-176129755 | Rare:94 | ||||
| chr2:176188524-176188668 | Common:1; Rare:51 | ||||
| chr2:177212427-177212821 | Common:4; Rare:158 | ||||
| chr2:177263410-177263595 | Rare:41 | ||||
| chr2:177264563-177264892 | Common:2; Rare:94 | ||||
| chr2:177392672-177393059 | Common:2; Rare:136; Clinvar:6; Clinvar (benign):4 | ||||
| chr2:177552761-177552838 | Common:1; Rare:29 | ||||
| chr2:177618706-177619018 | Common:7; Rare:85 | ||||
| chr2:178450731-178451024 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:178451090-178451300 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:180980280-180980545 | Common:1; Rare:86 | ||||
| chr2:181457344-181457536 | Common:2; Rare:73 | ||||
| chr2:181891665-181892111 | Common:4; Rare:180 | ||||
| chr2:182426702-182426792 | Rare:14 | ||||
| chr2:186485987-186486354 | Common:3; Rare:105 |