| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10249869-10250427 | Common:19; Rare:260; Clinvar:5; Clinvar (benign):2 | ||||
| chr5:10353590-10353910 | Common:3; Rare:119 | ||||
| chr5:10441827-10441886 | Rare:17 | ||||
| chr5:16465244-16465413 | Rare:54 | ||||
| chr5:16465426-16465920 | Common:1; Rare:137 | ||||
| chr5:31193502-31193698 | Common:3; Rare:37 | ||||
| chr5:31532037-31532352 | Common:3; Rare:88 | ||||
| chr5:32174254-32174403 | Common:1; Rare:56 | ||||
| chr5:32711102-32711334 | Rare:36 | ||||
| chr5:32712254-32712284 | Rare:6 | ||||
| chr5:33440617-33441125 | Common:7; Rare:141 | ||||
| chr5:34656065-34656435 | Common:4; Rare:102 | ||||
| chr5:34839278-34839352 | Common:2; Rare:22 | ||||
| chr5:34915486-34915733 | Common:1; Rare:57 | ||||
| chr5:34929671-34930021 | Common:1; Rare:109 |