| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:135578987-135579237 | Common:2; Rare:70 | ||||
| chr5:136132778-136132971 | Common:1; Rare:58 | ||||
| chr5:137753885-137753925 | Rare:9 | ||||
| chr5:137880501-137880641 | Common:1; Rare:23 | ||||
| chr5:137889312-137889424 | Common:1; Rare:42 | ||||
| chr5:138032693-138032780 | Common:1; Rare:20 | ||||
| chr5:138032964-138033175 | Common:1; Rare:72 | ||||
| chr5:138171088-138171409 | Common:1; Rare:78 | ||||
| chr5:138337982-138338283 | Common:1; Rare:113 | ||||
| chr5:138465815-138465914 | Rare:37 | ||||
| chr5:138542900-138543576 | Common:3; Rare:216 | ||||
| chr5:138575654-138575951 | Rare:83 | ||||
| chr5:138753220-138753507 | Common:2; Rare:98 | ||||
| chr5:138886112-138886292 | Rare:45 | ||||
| chr5:138930226-138930654 | Common:1; Rare:84; Clinvar (benign):1 |