| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:183987707-183987822 | Rare:17 | ||||
| chr4:184343953-184344049 | Rare:18 | ||||
| chr4:184815069-184815213 | Common:2; Rare:35 | ||||
| chr4:185734935-185735090 | Common:2; Rare:25 | ||||
| chr5:476078-476301 | Common:1; Rare:89 | ||||
| chr5:784721-784904 | Common:4; Rare:62 | ||||
| chr5:964124-964323 | Common:1; Rare:34 | ||||
| chr5:1633922-1634049 | Common:2; Rare:42 | ||||
| chr5:1883365-1883475 | Rare:24 | ||||
| chr5:1883829-1883975 | Common:1; Rare:26 | ||||
| chr5:1931038-1931274 | Common:3; Rare:56 | ||||
| chr5:1948620-1948992 | Common:9; Rare:80 | ||||
| chr5:8457586-8457761 | Common:2; Rare:54 | ||||
| chr5:34918104-34918386 | Common:2; Rare:51 | ||||
| chr5:37060624-37060993 | Common:3; Rare:64; Clinvar:1; Clinvar (benign):1 |