| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:137753828-137754156 | Rare:73 | ||||
| chr5:138033034-138033178 | Common:1; Rare:50 | ||||
| chr5:138178597-138178724 | Rare:33 | ||||
| chr5:138178953-138179154 | Common:1; Rare:43 | ||||
| chr5:138465689-138465725 | Common:1; Rare:14 | ||||
| chr5:138465815-138465929 | Rare:46 | ||||
| chr5:138542053-138542270 | Common:1; Rare:46 | ||||
| chr5:138543045-138543558 | Common:3; Rare:160 | ||||
| chr5:138557403-138557714 | Rare:72 | ||||
| chr5:138575261-138575452 | Common:1; Rare:103 | ||||
| chr5:138753255-138753507 | Common:2; Rare:87 | ||||
| chr5:138754003-138754206 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr5:138932277-138932710 | Common:3; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:139198277-139198521 | Rare:79; Clinvar (benign):1 | ||||
| chr5:139273950-139274142 | Rare:86 |