| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:76693052-76693438 | Common:2; Rare:73 | ||||
| chr5:76695218-76695530 | Rare:64 | ||||
| chr5:76874480-76874656 | Rare:37 | ||||
| chr5:77080558-77080788 | Common:1; Rare:52 | ||||
| chr5:77087919-77088123 | Common:2; Rare:43 | ||||
| chr5:78510353-78510490 | Rare:34 | ||||
| chr5:80442401-80442519 | Rare:17 | ||||
| chr5:87331218-87331447 | Common:1; Rare:65; Clinvar (benign):3 | ||||
| chr5:87332353-87332528 | Rare:37 | ||||
| chr5:87340656-87340934 | Common:1; Rare:51 | ||||
| chr5:87368481-87368695 | Rare:40 | ||||
| chr5:87369604-87369850 | Rare:36; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:87383846-87383849 | |||||
| chr5:87393075-87393107 | Rare:9 | ||||
| chr5:91314388-91314546 | Common:2; Rare:29 |