| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16465725-16465915 | Common:1; Rare:37 | ||||
| chr5:31532002-31532356 | Common:3; Rare:95 | ||||
| chr5:32174277-32174421 | Common:1; Rare:51 | ||||
| chr5:32444638-32444967 | Common:1; Rare:116 | ||||
| chr5:32585437-32585623 | Common:2; Rare:80 | ||||
| chr5:33440606-33441116 | Common:7; Rare:143 | ||||
| chr5:33891982-33892278 | Rare:65 | ||||
| chr5:34008015-34008280 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656102-34656473 | Common:3; Rare:103 | ||||
| chr5:34915208-34915360 | Rare:43 | ||||
| chr5:34915472-34915761 | Common:1; Rare:78 | ||||
| chr5:35617636-35617935 | Common:1; Rare:58 | ||||
| chr5:36151881-36152174 | Rare:91 | ||||
| chr5:38845712-38846067 | Common:2; Rare:94 | ||||
| chr5:39074373-39074522 | Common:1; Rare:67 |