| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:26947042-26947288 | Common:1; Rare:96 | ||||
| chr9:26947359-26947571 | Common:1; Rare:68 | ||||
| chr9:26956295-26956516 | Common:3; Rare:79 | ||||
| chr9:27297079-27297217 | Rare:36 | ||||
| chr9:27529624-27529799 | Common:4; Rare:40 | ||||
| chr9:27573422-27573530 | Common:5; Rare:56 | ||||
| chr9:27573709-27573972 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384491-32384732 | Common:1; Rare:91 | ||||
| chr9:32526167-32526384 | Common:4; Rare:70 | ||||
| chr9:32552005-32552380 | Common:2; Rare:105 | ||||
| chr9:32552541-32552633 | Common:1; Rare:17; Clinvar:2 | ||||
| chr9:32573000-32573243 | Common:3; Rare:84 | ||||
| chr9:32635520-32635763 | Rare:89 | ||||
| chr9:32783228-32783572 | Common:4; Rare:76 | ||||
| chr9:33001536-33001721 | Common:2; Rare:102; Clinvar (benign):4 |