| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:215436025-215436237 | Common:2; Rare:70 | ||||
| chr2:216081748-216081939 | Common:1; Rare:67 | ||||
| chr2:216498743-216498886 | Common:4; Rare:60 | ||||
| chr2:216694627-216694671 | Rare:14 | ||||
| chr2:217978797-217979110 | Common:3; Rare:89 | ||||
| chr2:217979234-217979535 | Common:3; Rare:40 | ||||
| chr2:218034863-218035000 | Common:2; Rare:34 | ||||
| chr2:218125966-218126369 | Common:2; Rare:67 | ||||
| chr2:218129136-218129342 | Rare:31 | ||||
| chr2:218166923-218167086 | Rare:26 | ||||
| chr2:218217057-218217246 | Common:1; Rare:67 | ||||
| chr2:218270003-218270544 | Common:5; Rare:174; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218279036-218279312 | Common:2; Rare:77 | ||||
| chr2:218287250-218287386 | Rare:24 | ||||
| chr2:218292477-218292648 | Common:1; Rare:52 |