| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:11343819-11343893 | Rare:14 | ||||
| chr2:11344582-11344889 | Common:2; Rare:124 | ||||
| chr2:11466095-11466245 | Common:5; Rare:48 | ||||
| chr2:11746461-11746679 | Common:2; Rare:68; Clinvar:5 | ||||
| chr2:12716747-12716952 | Common:1; Rare:52 | ||||
| chr2:15561247-15561450 | Rare:84 | ||||
| chr2:15591622-15591942 | Common:3; Rare:95 | ||||
| chr2:15591966-15592237 | Common:3; Rare:68 | ||||
| chr2:15592245-15592372 | Common:1; Rare:31 | ||||
| chr2:17518261-17518696 | Common:5; Rare:156 | ||||
| chr2:17753073-17753443 | Common:6; Rare:91 | ||||
| chr2:17753678-17753936 | Common:3; Rare:92 | ||||
| chr2:17754081-17754427 | Common:6; Rare:84; Clinvar (benign):1 | ||||
| chr2:18560036-18560312 | Common:1; Rare:89 | ||||
| chr2:18560378-18560454 | Rare:33 |