| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:69173871-69174411 | Common:12; Rare:320; Clinvar:4; Clinvar (benign):4 | ||||
| chr9:69759901-69760183 | Common:6; Rare:221 | ||||
| chr9:70258814-70259100 | Common:8; Rare:255 | ||||
| chr9:70414290-70414600 | Rare:112 | ||||
| chr9:71768791-71768955 | Common:1; Rare:46 | ||||
| chr9:71911143-71911725 | Common:6; Rare:317 | ||||
| chr9:72364160-72364770 | Common:7; Rare:259 | ||||
| chr9:72365147-72365423 | Common:4; Rare:192 | ||||
| chr9:74952146-74952429 | Rare:140 | ||||
| chr9:74952817-74952988 | Common:2; Rare:88 | ||||
| chr9:75027560-75028060 | Rare:209 | ||||
| chr9:75028209-75028661 | Common:6; Rare:232 | ||||
| chr9:75088086-75088602 | Common:8; Rare:343 | ||||
| chr9:76393920-76394130 | Common:2; Rare:143 | ||||
| chr9:76394240-76394750 | Common:16; Rare:303 |