| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:128091495-128091899 | Common:2; Rare:153 | ||||
| chr2:128318747-128319147 | Common:6; Rare:285 | ||||
| chr2:130129188-130129851 | Common:22; Rare:439 | ||||
| chr2:130180278-130181050 | Common:2; Rare:169 | ||||
| chr2:130181428-130181828 | Common:20; Rare:742 | ||||
| chr2:130181990-130182380 | Common:11; Rare:677 | ||||
| chr2:130183197-130183597 | Common:2; Rare:104 | ||||
| chr2:130341498-130341908 | Common:6; Rare:292 | ||||
| chr2:130342070-130342409 | Common:1; Rare:665; Clinvar:8; Clinvar (pathogenic):3 | ||||
| chr2:130342328-130342728 | Common:9; Rare:110 | ||||
| chr2:130342637-130343004 | Common:31; Rare:577 | ||||
| chr2:130343114-130343219 | Common:2; Rare:53 | ||||
| chr2:130343132-130343581 | Common:4; Rare:222 | ||||
| chr2:130355764-130356730 | Common:38; Rare:803 | ||||
| chr2:130371630-130372430 | Common:20; Rare:621 |