| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10761086-10761408 | Common:9; Rare:109 | ||||
| chr5:11903357-11903477 | Rare:23 | ||||
| chr5:14664572-14664718 | Common:3; Rare:68 | ||||
| chr5:16465709-16465949 | Common:1; Rare:56 | ||||
| chr5:16936235-16936437 | Common:3; Rare:53 | ||||
| chr5:31532045-31532351 | Common:3; Rare:87 | ||||
| chr5:32174252-32174413 | Common:1; Rare:60 | ||||
| chr5:33440617-33441117 | Common:7; Rare:140 | ||||
| chr5:34656113-34656435 | Common:3; Rare:86 | ||||
| chr5:34915487-34915741 | Common:1; Rare:57 | ||||
| chr5:34929538-34929862 | Rare:124 | ||||
| chr5:36151864-36152140 | Rare:77 | ||||
| chr5:36241622-36241857 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):4 | ||||
| chr5:36242162-36242407 | Common:1; Rare:67 | ||||
| chr5:36876642-36876894 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 |