| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:80407868-80408113 | Common:1; Rare:89 | ||||
| chr5:80487897-80488023 | Rare:36 | ||||
| chr5:80488042-80488157 | Rare:49 | ||||
| chr5:80654427-80654738 | Common:5; Rare:160 | ||||
| chr5:80960852-80960980 | Rare:34 | ||||
| chr5:81232902-81233361 | Common:2; Rare:94 | ||||
| chr5:81301467-81301685 | Common:5; Rare:74 | ||||
| chr5:81750985-81751162 | Rare:50 | ||||
| chr5:81971804-81972295 | Common:3; Rare:169 | ||||
| chr5:82278319-82278702 | Common:4; Rare:126 | ||||
| chr5:83077322-83077615 | Common:1; Rare:90 | ||||
| chr5:84384378-84384514 | Rare:39 | ||||
| chr5:84384593-84384719 | Rare:62 | ||||
| chr5:86617872-86618422 | Common:5; Rare:173 | ||||
| chr5:87267696-87268442 | Common:6; Rare:226; Clinvar:1; Clinvar (benign):2 |