| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3377791-3377953 | Rare:43 | ||||
| chr2:3379608-3379785 | Common:2; Rare:74 | ||||
| chr2:3519495-3519634 | Common:2; Rare:43 | ||||
| chr2:3558269-3558515 | Common:5; Rare:101 | ||||
| chr2:3575098-3575345 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):5 | ||||
| chr2:9423398-9423697 | Rare:92 | ||||
| chr2:9474455-9474587 | Common:7; Rare:56 | ||||
| chr2:9555699-9555898 | Common:2; Rare:66 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:9843277-9843533 | Common:6; Rare:76 | ||||
| chr2:10689934-10690006 | Common:2; Rare:22 | ||||
| chr2:12718178-12718239 | Common:1; Rare:11 | ||||
| chr2:15561298-15561375 | Rare:38 | ||||
| chr2:15940353-15940581 | Rare:55 | ||||
| chr2:17540443-17540802 | Common:2; Rare:78 |