| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35489722-35490108 | Common:1; Rare:114 | ||||
| chr9:35562974-35563196 | Rare:78 | ||||
| chr9:35657841-35658391 | Common:10; Rare:451; Clinvar:42; Clinvar (benign):16; Clinvar (pathogenic):40 | ||||
| chr9:35731983-35732331 | Common:2; Rare:89 | ||||
| chr9:35732373-35732676 | Common:2; Rare:76 | ||||
| chr9:35738792-35738982 | Rare:51; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr9:35748946-35749377 | Common:2; Rare:154 | ||||
| chr9:35749694-35749776 | Rare:33 | ||||
| chr9:35812149-35812267 | Rare:48 | ||||
| chr9:35814963-35815293 | Rare:82 | ||||
| chr9:36190681-36191063 | Common:2; Rare:120 | ||||
| chr9:36258409-36258622 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400841-36400997 | Common:3; Rare:70 | ||||
| chr9:37429615-37429764 | Common:2; Rare:60; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr9:37464970-37465139 | Common:2; Rare:57 |