| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:17216987-17217080 | Common:3; Rare:21 | ||||
| chr5:17217088-17217177 | Common:2; Rare:17 | ||||
| chr5:17217306-17217804 | Common:6; Rare:90 | ||||
| chr5:24644695-24644829 | Common:3; Rare:18 | ||||
| chr5:24644898-24644989 | Rare:21 | ||||
| chr5:31532032-31532356 | Common:3; Rare:90 | ||||
| chr5:31854790-31854970 | Common:1; Rare:62 | ||||
| chr5:32174307-32174402 | Common:1; Rare:32 | ||||
| chr5:32444620-32444859 | Common:1; Rare:90 | ||||
| chr5:32711046-32711321 | Common:1; Rare:45 | ||||
| chr5:33440600-33441058 | Common:6; Rare:119 | ||||
| chr5:34008027-34008231 | Common:2; Rare:80; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656133-34656474 | Common:3; Rare:88 | ||||
| chr5:34657228-34657412 | Common:2; Rare:38 | ||||
| chr5:34839082-34839179 | Rare:31 |