| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:36598071-36598284 | Common:15; Rare:94 | ||||
| chr2:36965964-36966203 | Rare:65 | ||||
| chr2:36966582-36966868 | Common:3; Rare:128 | ||||
| chr2:37084272-37084544 | Common:3; Rare:97 | ||||
| chr2:37156944-37157061 | Common:1; Rare:39 | ||||
| chr2:37231477-37231714 | Common:5; Rare:127; Clinvar (benign):3 | ||||
| chr2:37324515-37324950 | Common:3; Rare:149 | ||||
| chr2:37672088-37672329 | Common:5; Rare:62 | ||||
| chr2:37672560-37672920 | Common:4; Rare:103 | ||||
| chr2:37925070-37925280 | Common:2; Rare:70 | ||||
| chr2:37925347-37925586 | Common:4; Rare:113 | ||||
| chr2:38076290-38076620 | Common:5; Rare:72 | ||||
| chr2:38076640-38077210 | Common:2; Rare:156 | ||||
| chr2:38376277-38377020 | Common:5; Rare:306 | ||||
| chr2:38377202-38377519 | Common:3; Rare:135 |