| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:32712238-32712284 | Rare:9 | ||||
| chr5:33440597-33441125 | Common:7; Rare:146 | ||||
| chr5:34008006-34008212 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656150-34656473 | Common:3; Rare:82 | ||||
| chr5:34839045-34839190 | Rare:51 | ||||
| chr5:34839237-34839407 | Common:2; Rare:51 | ||||
| chr5:34915216-34915287 | Rare:19 | ||||
| chr5:34915461-34915753 | Common:1; Rare:76 | ||||
| chr5:35230333-35230402 | Common:1; Rare:15 | ||||
| chr5:35230429-35230632 | Rare:38 | ||||
| chr5:35230646-35230768 | Rare:23 | ||||
| chr5:36151803-36152161 | Rare:93 | ||||
| chr5:36241556-36241961 | Common:5; Rare:143; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36606476-36606660 | Rare:31 | ||||
| chr5:36876642-36876938 | Common:1; Rare:86; Clinvar:1; Clinvar (benign):1 |