| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216695219-216695309 | Common:1; Rare:17 | ||||
| chr2:216695321-216695590 | Rare:49 | ||||
| chr2:217813855-217813866 | Common:1; Rare:2 | ||||
| chr2:218216918-218217389 | Common:3; Rare:141 | ||||
| chr2:218233391-218233441 | Common:1; Rare:5 | ||||
| chr2:218270104-218270532 | Common:5; Rare:130; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218286726-218287013 | Common:1; Rare:51 | ||||
| chr2:218399931-218400144 | Rare:78 | ||||
| chr2:218568209-218568698 | Common:6; Rare:122 | ||||
| chr2:218568731-218568985 | Common:1; Rare:69 | ||||
| chr2:218659283-218659367 | Common:1; Rare:18 | ||||
| chr2:218659583-218659762 | Rare:45 | ||||
| chr2:218661232-218661505 | Rare:78; Clinvar:8; Clinvar (pathogenic):3 | ||||
| chr2:218671932-218672348 | Common:2; Rare:121 | ||||
| chr2:218693486-218693785 | Common:1; Rare:60 |