| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915461-34915783 | Common:1; Rare:92 | ||||
| chr5:35856869-35856935 | Rare:9 | ||||
| chr5:36151859-36152203 | Rare:105 | ||||
| chr5:36241624-36241826 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):3 | ||||
| chr5:36242126-36242346 | Common:1; Rare:60 | ||||
| chr5:36876625-36876868 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 | ||||
| chr5:36877102-36877149 | Rare:18 | ||||
| chr5:37371053-37371189 | Rare:50 | ||||
| chr5:37379179-37379351 | Rare:41 | ||||
| chr5:39074381-39074489 | Common:1; Rare:44 | ||||
| chr5:40755889-40756077 | Rare:50 | ||||
| chr5:40798166-40798435 | Common:1; Rare:104 | ||||
| chr5:40835165-40835417 | Common:2; Rare:103 | ||||
| chr5:41870364-41870553 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41904029-41904371 | Common:1; Rare:101 |