| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95086512-95086571 | Common:1; Rare:12 | ||||
| chr9:96345370-96345471 | Rare:20 | ||||
| chr9:96351677-96351995 | Common:1; Rare:53 | ||||
| chr9:96947035-96947313 | Common:4; Rare:36 | ||||
| chr9:97238280-97238519 | Common:4; Rare:70 | ||||
| chr9:97238662-97238939 | Common:2; Rare:60 | ||||
| chr9:97669436-97669698 | Common:2; Rare:58 | ||||
| chr9:97798889-97799091 | Common:2; Rare:20 | ||||
| chr9:97856316-97856539 | Common:1; Rare:31 | ||||
| chr9:98015151-98015401 | Rare:41 | ||||
| chr9:99137687-99138022 | Common:1; Rare:52; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr9:99978911-99979008 | Rare:13 | ||||
| chr9:100180499-100180702 | Common:1; Rare:33 | ||||
| chr9:100305699-100305981 | Rare:51 | ||||
| chr9:100306204-100306250 | Rare:7 |