| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:137754725-137754855 | Rare:47 | ||||
| chr5:137889287-137889484 | Common:1; Rare:79 | ||||
| chr5:138033006-138033187 | Common:1; Rare:67 | ||||
| chr5:138178598-138178720 | Rare:32 | ||||
| chr5:138178927-138179190 | Common:3; Rare:54 | ||||
| chr5:138213275-138213525 | Rare:69 | ||||
| chr5:138331753-138332142 | Common:2; Rare:98 | ||||
| chr5:138338115-138338296 | Common:2; Rare:78 | ||||
| chr5:138542839-138543044 | Rare:59 | ||||
| chr5:138543070-138543569 | Common:3; Rare:160 | ||||
| chr5:138575008-138575128 | Common:2; Rare:30 | ||||
| chr5:138575225-138575482 | Common:1; Rare:125 | ||||
| chr5:138575654-138575821 | Rare:44 | ||||
| chr5:138753248-138753507 | Common:2; Rare:89 | ||||
| chr5:138875256-138875415 | Rare:25; Clinvar (benign):1 |