| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80407864-80408130 | Common:1; Rare:94 | ||||
| chr5:80487913-80488132 | Common:1; Rare:70 | ||||
| chr5:80654535-80654738 | Common:5; Rare:121 | ||||
| chr5:80654914-80655186 | Common:5; Rare:103; Clinvar (benign):2 | ||||
| chr5:81301462-81301710 | Common:5; Rare:86 | ||||
| chr5:81750985-81751345 | Common:1; Rare:99 | ||||
| chr5:81971752-81972295 | Common:4; Rare:187 | ||||
| chr5:82278319-82278711 | Common:4; Rare:129 | ||||
| chr5:83077321-83077639 | Common:1; Rare:99 | ||||
| chr5:83077827-83078079 | Common:2; Rare:52 | ||||
| chr5:83471380-83472041 | Common:4; Rare:157; Clinvar:4; Clinvar (benign):1 | ||||
| chr5:86617769-86618181 | Common:2; Rare:141 | ||||
| chr5:87267722-87268063 | Common:4; Rare:110 | ||||
| chr5:87268598-87268889 | Common:1; Rare:136; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr5:87412801-87412966 | Common:3; Rare:57 |