| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:79069534-79069814 | Rare:98; Clinvar (benign):3 | ||||
| chr5:79111569-79111820 | Rare:57 | ||||
| chr5:79235992-79236102 | Common:1; Rare:47 | ||||
| chr5:79612237-79612625 | Rare:107 | ||||
| chr5:79991231-79991337 | Rare:31 | ||||
| chr5:80255994-80256277 | Common:2; Rare:111 | ||||
| chr5:80407868-80408103 | Common:1; Rare:87 | ||||
| chr5:80487895-80488124 | Common:1; Rare:73 | ||||
| chr5:80654514-80654738 | Common:5; Rare:133 | ||||
| chr5:81233009-81233335 | Common:1; Rare:68 | ||||
| chr5:81301449-81301698 | Common:5; Rare:86 | ||||
| chr5:81301900-81302004 | Common:2; Rare:20 | ||||
| chr5:81394020-81394208 | Common:3; Rare:48 | ||||
| chr5:81971853-81972048 | Common:2; Rare:75 | ||||
| chr5:82278319-82278681 | Common:3; Rare:116 |