| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:78648505-78648665 | Common:3; Rare:38 | ||||
| chr5:78648703-78649077 | Common:2; Rare:117 | ||||
| chr5:79069580-79069795 | Rare:72; Clinvar (benign):2 | ||||
| chr5:79236008-79236135 | Common:1; Rare:49 | ||||
| chr5:79612259-79612701 | Rare:126 | ||||
| chr5:79991067-79991363 | Rare:103 | ||||
| chr5:80255977-80256271 | Common:1; Rare:114 | ||||
| chr5:80407362-80407612 | Common:2; Rare:44 | ||||
| chr5:80407824-80408100 | Common:1; Rare:106 | ||||
| chr5:80487888-80488132 | Common:1; Rare:77 | ||||
| chr5:80654463-80654738 | Common:5; Rare:151 | ||||
| chr5:80654981-80655185 | Common:1; Rare:60 | ||||
| chr5:81233268-81233347 | Rare:24 | ||||
| chr5:81301470-81301685 | Common:5; Rare:72 | ||||
| chr5:81751104-81751448 | Common:1; Rare:98 |