| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15472602-15472862 | Rare:78 | ||||
| chr9:15552774-15553236 | Common:4; Rare:171 | ||||
| chr9:15553377-15553514 | Common:2; Rare:34 | ||||
| chr9:16870661-16870812 | Rare:69 | ||||
| chr9:17134909-17135176 | Common:1; Rare:128 | ||||
| chr9:18473944-18474223 | Rare:75 | ||||
| chr9:19049291-19049638 | Common:2; Rare:137 | ||||
| chr9:19102843-19103094 | Common:2; Rare:106 | ||||
| chr9:19380178-19380403 | Common:5; Rare:111 | ||||
| chr9:19408773-19408936 | Common:4; Rare:64 | ||||
| chr9:20658199-20658365 | Common:3; Rare:62 | ||||
| chr9:20684074-20684283 | Common:3; Rare:82 | ||||
| chr9:21335374-21335528 | Common:2; Rare:53 | ||||
| chr9:21802513-21802677 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994344-21994842 | Common:2; Rare:146; Clinvar:1; Clinvar (benign):4 |