| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:33891982-33892279 | Rare:65 | ||||
| chr5:34007997-34008214 | Common:2; Rare:81; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656110-34656418 | Common:3; Rare:85 | ||||
| chr5:34838932-34839196 | Common:2; Rare:83 | ||||
| chr5:34839278-34839419 | Common:2; Rare:45 | ||||
| chr5:34915497-34915761 | Common:1; Rare:68 | ||||
| chr5:35617713-35617921 | Common:1; Rare:37 | ||||
| chr5:36151881-36152203 | Rare:102 | ||||
| chr5:36606476-36606622 | Rare:25 | ||||
| chr5:36876650-36876885 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:37371048-37371379 | Common:2; Rare:80 | ||||
| chr5:37379156-37379351 | Common:1; Rare:45 | ||||
| chr5:39074373-39074539 | Common:1; Rare:76 | ||||
| chr5:39425099-39425280 | Common:2; Rare:46 | ||||
| chr5:40798152-40798448 | Common:1; Rare:116 |