| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:87339805-87340032 | Rare:25 | ||||
| chr5:87341469-87341724 | Common:1; Rare:39 | ||||
| chr5:87362370-87362671 | Common:1; Rare:62; Clinvar:2; Clinvar (benign):3 | ||||
| chr5:87366969-87367025 | Rare:9 | ||||
| chr5:87368457-87368651 | Rare:36 | ||||
| chr5:87375156-87375203 | Rare:7 | ||||
| chr5:87380988-87381270 | Rare:51 | ||||
| chr5:87383692-87383948 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:87386661-87386903 | Common:2; Rare:53 | ||||
| chr5:87409287-87409426 | Common:1; Rare:49 | ||||
| chr5:91314396-91314558 | Common:2; Rare:28 | ||||
| chr5:91376194-91376485 | Rare:51 | ||||
| chr5:93411342-93411447 | Rare:15 | ||||
| chr5:93490858-93491062 | Common:1; Rare:25 | ||||
| chr5:93521048-93521117 | Common:2; Rare:7 |