| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73565370-73565810 | Common:7; Rare:135 | ||||
| chr5:74640470-74640659 | Common:1; Rare:47 | ||||
| chr5:74767043-74767308 | Common:2; Rare:78 | ||||
| chr5:75336919-75337294 | Common:3; Rare:129 | ||||
| chr5:75511597-75511941 | Common:1; Rare:121 | ||||
| chr5:76083271-76083410 | Common:2; Rare:33 | ||||
| chr5:76403037-76403594 | Common:2; Rare:150 | ||||
| chr5:76715878-76716179 | Common:7; Rare:89 | ||||
| chr5:76818752-76819136 | Common:3; Rare:101 | ||||
| chr5:77030253-77030501 | Common:1; Rare:90 | ||||
| chr5:78294455-78294553 | Rare:27 | ||||
| chr5:78360355-78360702 | Common:5; Rare:132 | ||||
| chr5:78648729-78649041 | Common:2; Rare:104 | ||||
| chr5:79069627-79069777 | Rare:52; Clinvar (benign):2 | ||||
| chr5:79235945-79236135 | Common:2; Rare:79 |