| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:31400599-31400760 | Common:5; Rare:31 | ||||
| chr6:31720316-31720396 | Rare:10 | ||||
| chr6:31779270-31779440 | Rare:45 | ||||
| chr6:32179532-32179739 | Common:1; Rare:52 | ||||
| chr6:32222891-32223100 | Common:1; Rare:55 | ||||
| chr6:32894520-32894832 | Common:12; Rare:86 | ||||
| chr6:33425670-33425875 | Common:1; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:35469855-35470274 | Common:4; Rare:96 | ||||
| chr6:35670279-35670505 | Rare:31 | ||||
| chr6:36756319-36756451 | Rare:37 | ||||
| chr6:37170942-37171188 | Rare:92 | ||||
| chr6:39821050-39821258 | Common:2; Rare:41 | ||||
| chr6:39999129-39999326 | Common:2; Rare:44 | ||||
| chr6:42126233-42126509 | Common:10; Rare:52 | ||||
| chr6:42139992-42140268 | Common:2; Rare:46 |