| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:216412222-216412538 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr2:216498743-216498985 | Common:9; Rare:103 | ||||
| chr2:218217064-218217226 | Common:1; Rare:61 | ||||
| chr2:218270082-218270538 | Common:5; Rare:144; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218322988-218323275 | Common:6; Rare:93 | ||||
| chr2:218568290-218568618 | Common:2; Rare:88 | ||||
| chr2:218568726-218568961 | Common:1; Rare:66 | ||||
| chr2:218659594-218659738 | Rare:34 | ||||
| chr2:218671976-218672334 | Common:2; Rare:89 | ||||
| chr2:218710707-218710897 | Common:2; Rare:54 | ||||
| chr2:219176914-219177073 | Common:4; Rare:49 | ||||
| chr2:219206681-219206990 | Rare:109 | ||||
| chr2:219229555-219229905 | Common:2; Rare:113 | ||||
| chr2:219245424-219245531 | Rare:33 | ||||
| chr2:219253904-219254097 | Common:2; Rare:61 |