| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138337736-138338061 | Common:3; Rare:88 | ||||
| chr5:138338065-138338134 | Rare:29 | ||||
| chr5:138338203-138338289 | Common:1; Rare:40 | ||||
| chr5:138543104-138543569 | Common:2; Rare:153 | ||||
| chr5:138557368-138557737 | Common:1; Rare:92 | ||||
| chr5:138557868-138558082 | Rare:57 | ||||
| chr5:138575271-138575956 | Common:2; Rare:242 | ||||
| chr5:138611356-138611451 | Common:3; Rare:24 | ||||
| chr5:138753277-138753503 | Common:2; Rare:77 | ||||
| chr5:138875289-138875486 | Rare:39; Clinvar (benign):1 | ||||
| chr5:138953462-138953764 | Common:3; Rare:60 | ||||
| chr5:139198258-139198538 | Rare:89; Clinvar (benign):1 | ||||
| chr5:139273975-139274156 | Rare:85 | ||||
| chr5:139293581-139293861 | Rare:86 | ||||
| chr5:139294434-139294734 | Common:1; Rare:97 |