| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519465-3519617 | Common:2; Rare:55 | ||||
| chr2:3558225-3558658 | Common:6; Rare:165 | ||||
| chr2:3575098-3575385 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):6 | ||||
| chr2:9003974-9004120 | Rare:67 | ||||
| chr2:9423140-9423763 | Common:1; Rare:172 | ||||
| chr2:9474508-9474630 | Common:6; Rare:58 | ||||
| chr2:9555621-9555992 | Common:2; Rare:122 | ||||
| chr2:9630950-9631346 | Common:3; Rare:127 | ||||
| chr2:9843249-9843515 | Common:6; Rare:76 | ||||
| chr2:9843645-9843721 | Common:2; Rare:29 | ||||
| chr2:10689919-10689997 | Common:2; Rare:25 | ||||
| chr2:11746501-11746648 | Common:1; Rare:46; Clinvar:2 | ||||
| chr2:12716621-12716959 | Common:3; Rare:105 | ||||
| chr2:17540416-17540819 | Common:2; Rare:89 | ||||
| chr2:17753721-17754174 | Common:4; Rare:143; Clinvar (benign):1 |