| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:218217058-218217383 | Common:2; Rare:105 | ||||
| chr2:218270095-218270532 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:218287241-218287411 | Rare:28 | ||||
| chr2:218292456-218292630 | Common:1; Rare:48 | ||||
| chr2:218399645-218399903 | Rare:120 | ||||
| chr2:218568256-218568702 | Common:5; Rare:114 | ||||
| chr2:218568731-218568974 | Common:1; Rare:68 | ||||
| chr2:218659306-218659793 | Common:4; Rare:123 | ||||
| chr2:218671933-218672137 | Rare:82 | ||||
| chr2:219176893-219177015 | Common:3; Rare:36 | ||||
| chr2:219178146-219178284 | Common:6; Rare:83 | ||||
| chr2:219217740-219218032 | Common:1; Rare:69; Clinvar:2 | ||||
| chr2:219229055-219229395 | Common:2; Rare:80 | ||||
| chr2:219229541-219229953 | Common:3; Rare:121 | ||||
| chr2:219245401-219245539 | Common:1; Rare:40 |