| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:79069524-79069812 | Rare:101; Clinvar (benign):3 | ||||
| chr5:79082865-79083281 | Common:4; Rare:101 | ||||
| chr5:79111472-79111918 | Rare:118 | ||||
| chr5:79236013-79236128 | Common:1; Rare:45 | ||||
| chr5:79991186-79991313 | Rare:42 | ||||
| chr5:80255977-80256257 | Common:1; Rare:111 | ||||
| chr5:80407868-80408103 | Common:1; Rare:87 | ||||
| chr5:80487887-80488118 | Common:1; Rare:73 | ||||
| chr5:80654562-80654738 | Common:5; Rare:112 | ||||
| chr5:81233175-81233335 | Rare:44 | ||||
| chr5:81301440-81301685 | Common:5; Rare:81 | ||||
| chr5:81393990-81394222 | Common:4; Rare:60 | ||||
| chr5:81971784-81972057 | Common:3; Rare:108 | ||||
| chr5:82278319-82278681 | Common:3; Rare:116 | ||||
| chr5:83077330-83077615 | Common:1; Rare:85 |