| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244573-26244984 | Common:2; Rare:152; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345798-26346160 | Common:1; Rare:109 | ||||
| chr2:27032852-27033009 | Rare:63 | ||||
| chr2:27051546-27051727 | Rare:57 | ||||
| chr2:27071604-27072085 | Common:2; Rare:133 | ||||
| chr2:27211794-27212065 | Common:3; Rare:93 | ||||
| chr2:27212232-27212387 | Common:2; Rare:82 | ||||
| chr2:27217296-27217503 | Rare:85 | ||||
| chr2:27263031-27263302 | Common:1; Rare:59 | ||||
| chr2:27275294-27275467 | Common:1; Rare:56 | ||||
| chr2:27323040-27323145 | Rare:29; Clinvar (benign):1 | ||||
| chr2:27356748-27357199 | Common:2; Rare:136 | ||||
| chr2:27370259-27370641 | Common:1; Rare:158 | ||||
| chr2:27442218-27442417 | Rare:70 | ||||
| chr2:27489673-27489935 | Rare:65; Clinvar (benign):1 |