| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:137753828-137753899 | Rare:12 | ||||
| chr5:138032999-138033175 | Common:1; Rare:62 | ||||
| chr5:138338230-138338277 | Common:1; Rare:27 | ||||
| chr5:138465010-138465194 | Rare:42 | ||||
| chr5:138465550-138466068 | Common:1; Rare:193 | ||||
| chr5:138543024-138543513 | Common:3; Rare:145 | ||||
| chr5:138557400-138557667 | Rare:65 | ||||
| chr5:138753254-138753507 | Common:2; Rare:88 | ||||
| chr5:138930373-138930678 | Common:1; Rare:64; Clinvar (benign):1 | ||||
| chr5:138932367-138932710 | Common:2; Rare:83; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:139273975-139274140 | Rare:77 | ||||
| chr5:139384474-139384650 | Common:1; Rare:48 | ||||
| chr5:139462675-139462827 | Rare:31 | ||||
| chr5:139561100-139561437 | Common:1; Rare:136 | ||||
| chr5:139561734-139561826 | Rare:32 |