| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:73120489-73120624 | Common:1; Rare:34 | ||||
| chr5:73498345-73498501 | Common:1; Rare:43 | ||||
| chr5:73565597-73565743 | Common:3; Rare:57 | ||||
| chr5:74685121-74685242 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2 | ||||
| chr5:74767047-74767327 | Common:2; Rare:82 | ||||
| chr5:75511611-75511913 | Common:1; Rare:112 | ||||
| chr5:77087201-77087464 | Rare:43 | ||||
| chr5:78360391-78360649 | Common:5; Rare:100 | ||||
| chr5:79069509-79069554 | Rare:11; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr5:79236031-79236173 | Common:1; Rare:54 | ||||
| chr5:80407859-80408096 | Common:1; Rare:87 | ||||
| chr5:80487938-80488011 | Rare:19 | ||||
| chr5:81301513-81301668 | Common:4; Rare:55 | ||||
| chr5:82278328-82278665 | Common:3; Rare:106 | ||||
| chr5:83077339-83077618 | Common:1; Rare:80 |