| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104094425-104094603 | Common:2; Rare:48 | ||||
| chr9:104747555-104747811 | Common:1; Rare:78 | ||||
| chr9:104764004-104764277 | Common:2; Rare:76 | ||||
| chr9:105447976-105448189 | Common:2; Rare:78 | ||||
| chr9:105558082-105558339 | Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862412-106862753 | Common:4; Rare:87 | ||||
| chr9:106862896-106863186 | Rare:86 | ||||
| chr9:106863286-106863642 | Common:1; Rare:77 | ||||
| chr9:108933911-108934025 | Common:2; Rare:41; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:108934042-108934532 | Common:8; Rare:192; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109498230-109498423 | Rare:65 | ||||
| chr9:109867145-109867571 | Common:10; Rare:107 | ||||
| chr9:110125345-110125513 | Rare:31 | ||||
| chr9:111525065-111525257 | Common:5; Rare:59 | ||||
| chr9:111599787-111599886 | Common:1; Rare:33 |