| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104747535-104747784 | Common:1; Rare:73 | ||||
| chr9:104764045-104764185 | Common:2; Rare:34 | ||||
| chr9:104928141-104928464 | Common:6; Rare:84; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105244349-105244876 | Common:4; Rare:178 | ||||
| chr9:105447955-105448189 | Common:2; Rare:87 | ||||
| chr9:105558057-105558163 | Rare:33; Clinvar (benign):1 | ||||
| chr9:106862942-106863180 | Rare:76 | ||||
| chr9:106863312-106863646 | Common:1; Rare:71 | ||||
| chr9:107282967-107283357 | Common:2; Rare:131 | ||||
| chr9:107488214-107488633 | Common:2; Rare:124 | ||||
| chr9:107488653-107488916 | Common:1; Rare:90 | ||||
| chr9:107489749-107490034 | Common:3; Rare:117 | ||||
| chr9:108934029-108934493 | Common:7; Rare:183; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498226-109498457 | Rare:73 | ||||
| chr9:110148516-110148670 | Common:1; Rare:32 |