| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73625869-73626267 | Common:4; Rare:96 | ||||
| chr5:74632519-74632569 | Rare:11 | ||||
| chr5:74640490-74640667 | Common:1; Rare:47 | ||||
| chr5:74640714-74640850 | Common:1; Rare:38 | ||||
| chr5:74685099-74685446 | Common:3; Rare:134; Clinvar:6; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr5:74685478-74685556 | Rare:17 | ||||
| chr5:74767007-74767363 | Common:3; Rare:109 | ||||
| chr5:74866300-74866585 | Common:1; Rare:84 | ||||
| chr5:75236858-75236979 | Common:6; Rare:53 | ||||
| chr5:75336339-75336530 | Common:1; Rare:37 | ||||
| chr5:75336958-75337290 | Common:3; Rare:111 | ||||
| chr5:75511606-75511943 | Common:1; Rare:120 | ||||
| chr5:75696075-75696266 | Common:5; Rare:52 | ||||
| chr5:75717320-75717672 | Common:5; Rare:91 | ||||
| chr5:76623234-76623512 | Common:2; Rare:69 |