| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:6378498-6378686 | Rare:75 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9545954-9546366 | Common:10; Rare:101 | ||||
| chr5:10249869-10250157 | Common:16; Rare:138 | ||||
| chr5:10353597-10353913 | Common:3; Rare:115 | ||||
| chr5:14664572-14664695 | Common:2; Rare:54 | ||||
| chr5:16465706-16465902 | Rare:37 | ||||
| chr5:16935832-16935927 | Common:1; Rare:37 | ||||
| chr5:27120674-27120689 | Rare:10 | ||||
| chr5:31193616-31193698 | Rare:9 | ||||
| chr5:31532037-31532356 | Common:3; Rare:88 | ||||
| chr5:32174277-32174389 | Common:1; Rare:42 | ||||
| chr5:32710542-32710702 | Common:1; Rare:37 | ||||
| chr5:32711164-32711334 | Rare:28 | ||||
| chr5:33440593-33441076 | Common:6; Rare:127 |