| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:94259294-94259411 | Common:1; Rare:30 | ||||
| chr9:94374290-94374602 | Common:2; Rare:105 | ||||
| chr9:94726515-94726750 | Common:1; Rare:67 | ||||
| chr9:95004374-95004488 | Common:1; Rare:21 | ||||
| chr9:95048521-95049197 | Common:2; Rare:254 | ||||
| chr9:95055599-95056374 | Rare:164 | ||||
| chr9:95315991-95316620 | Common:6; Rare:171 | ||||
| chr9:95316842-95317060 | Common:2; Rare:57 | ||||
| chr9:95317118-95317559 | Common:6; Rare:137; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:95317630-95317870 | Common:1; Rare:75; Clinvar:2 | ||||
| chr9:95509082-95509475 | Rare:98 | ||||
| chr9:95516762-95516922 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
| chr9:95875393-95875691 | Rare:94 | ||||
| chr9:95875958-95876130 | Common:6; Rare:79; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96383540-96383980 | Common:4; Rare:125 |