| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26033799-26034151 | Common:3; Rare:120 | ||||
| chr2:26034267-26034732 | Common:4; Rare:111 | ||||
| chr2:26244530-26245031 | Common:2; Rare:174; Clinvar:7; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:26345800-26346210 | Common:1; Rare:125 | ||||
| chr2:26764194-26764352 | Common:2; Rare:62 | ||||
| chr2:27032862-27033005 | Rare:55 | ||||
| chr2:27071498-27071878 | Common:1; Rare:113 | ||||
| chr2:27086537-27086797 | Common:3; Rare:76; Clinvar (benign):1 | ||||
| chr2:27211775-27212109 | Common:3; Rare:117 | ||||
| chr2:27212252-27212437 | Common:2; Rare:97 | ||||
| chr2:27323050-27323162 | Rare:30; Clinvar (benign):1 | ||||
| chr2:27356750-27357170 | Common:2; Rare:121 | ||||
| chr2:27370297-27370780 | Common:2; Rare:189 | ||||
| chr2:27380762-27380912 | Common:1; Rare:46 | ||||
| chr2:27582961-27583101 | Rare:51 |