| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36258326-36258610 | Common:3; Rare:65; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37592536-37592643 | Common:2; Rare:38 | ||||
| chr9:37785043-37785134 | Common:1; Rare:33; Clinvar (benign):2 | ||||
| chr9:37800707-37800830 | Rare:38 | ||||
| chr9:37904063-37904441 | Common:3; Rare:126 | ||||
| chr9:69759896-69760073 | Common:2; Rare:81 | ||||
| chr9:70258842-70259076 | Common:3; Rare:109 | ||||
| chr9:70413914-70414157 | Rare:46 | ||||
| chr9:70414297-70414511 | Rare:52 | ||||
| chr9:71911167-71911525 | Common:3; Rare:108 | ||||
| chr9:72364500-72364857 | Common:4; Rare:119 | ||||
| chr9:72577241-72577425 | Common:1; Rare:26 | ||||
| chr9:72577493-72577788 | Common:1; Rare:52 | ||||
| chr9:73157129-73157425 | Common:2; Rare:54 | ||||
| chr9:75088100-75088698 | Common:4; Rare:197 |