| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73498321-73499203 | Common:5; Rare:254 | ||||
| chr5:73565286-73565837 | Common:8; Rare:163 | ||||
| chr5:74685073-74685253 | Common:3; Rare:63; Clinvar:2; Clinvar (benign):2 | ||||
| chr5:74766948-74767363 | Common:3; Rare:124 | ||||
| chr5:74865785-74865820 | Rare:12 | ||||
| chr5:74865880-74865919 | Rare:5 | ||||
| chr5:74866149-74866276 | Rare:38 | ||||
| chr5:74866754-74867099 | Common:2; Rare:76 | ||||
| chr5:75336857-75337300 | Common:4; Rare:146 | ||||
| chr5:75350137-75350374 | Rare:54 | ||||
| chr5:75511579-75511917 | Common:1; Rare:118 | ||||
| chr5:75611233-75611479 | Common:1; Rare:61 | ||||
| chr5:75717320-75717690 | Common:6; Rare:99 | ||||
| chr5:76403038-76403356 | Rare:82 | ||||
| chr5:77086596-77087025 | Common:4; Rare:84 |