| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95004449-95004496 | Rare:12 | ||||
| chr9:95317653-95317750 | Rare:37; Clinvar:2 | ||||
| chr9:95494059-95494221 | Common:1; Rare:48 | ||||
| chr9:95875429-95875729 | Common:1; Rare:108 | ||||
| chr9:95875969-95876068 | Common:5; Rare:51; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383522-96383810 | Common:3; Rare:97 | ||||
| chr9:96449920-96450306 | Common:4; Rare:134 | ||||
| chr9:96566876-96567183 | Rare:77 | ||||
| chr9:96655089-96655292 | Common:1; Rare:61 | ||||
| chr9:96655307-96655364 | Rare:15 | ||||
| chr9:97411906-97412231 | Common:4; Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:97633261-97633912 | Common:7; Rare:195 | ||||
| chr9:97922179-97922320 | Common:1; Rare:50 | ||||
| chr9:97922450-97922611 | Common:3; Rare:81 | ||||
| chr9:98255600-98255899 | Common:3; Rare:92 |