| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216081756-216081973 | Common:1; Rare:68 | ||||
| chr2:216082943-216083073 | Rare:18 | ||||
| chr2:216412272-216412597 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:216412694-216412791 | Rare:12 | ||||
| chr2:216498711-216498977 | Common:10; Rare:112 | ||||
| chr2:217433655-217433916 | Rare:49 | ||||
| chr2:217434088-217434386 | Rare:63 | ||||
| chr2:217756517-217756623 | Common:1; Rare:26 | ||||
| chr2:218217040-218217253 | Common:1; Rare:74 | ||||
| chr2:218270091-218270573 | Common:5; Rare:155; Clinvar:5; Clinvar (benign):2 | ||||
| chr2:218568190-218568708 | Common:6; Rare:133 | ||||
| chr2:218568733-218568966 | Common:1; Rare:65 | ||||
| chr2:218659339-218659785 | Common:4; Rare:112 | ||||
| chr2:218671971-218672348 | Common:2; Rare:95 | ||||
| chr2:218710701-218710997 | Common:3; Rare:70 |