| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27356094-27356115 | Rare:10 | ||||
| chr2:27356139-27356321 | Common:1; Rare:40 | ||||
| chr2:27356403-27356577 | Rare:64 | ||||
| chr2:27356593-27357329 | Common:3; Rare:210 | ||||
| chr2:27370017-27370172 | Common:2; Rare:46 | ||||
| chr2:27370227-27370689 | Common:2; Rare:187 | ||||
| chr2:27380486-27380631 | Rare:50; Clinvar:5 | ||||
| chr2:27380663-27381108 | Common:1; Rare:148; Clinvar:2 | ||||
| chr2:27409491-27409854 | Rare:128 | ||||
| chr2:27428310-27428809 | Common:1; Rare:164 | ||||
| chr2:27428918-27429388 | Common:3; Rare:127 | ||||
| chr2:27442338-27442650 | Common:1; Rare:149 | ||||
| chr2:27442848-27442939 | Rare:38 | ||||
| chr2:27443062-27443119 | Rare:22 | ||||
| chr2:27489625-27490044 | Common:1; Rare:112; Clinvar (benign):1 |