| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:106862793-106862910 | Rare:28 | ||||
| chr9:106862916-106863198 | Rare:87 | ||||
| chr9:106863524-106863679 | Common:1; Rare:29 | ||||
| chr9:107282940-107283286 | Common:3; Rare:122 | ||||
| chr9:107283985-107284125 | Common:1; Rare:40 | ||||
| chr9:107488428-107488633 | Common:1; Rare:58 | ||||
| chr9:107489767-107490061 | Common:4; Rare:127 | ||||
| chr9:108933902-108933965 | Common:2; Rare:22; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:108933969-108934018 | Rare:17; Clinvar:1 | ||||
| chr9:108934029-108934532 | Common:8; Rare:197; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:109013351-109013531 | Common:2; Rare:64 | ||||
| chr9:109119378-109119594 | Common:3; Rare:82 | ||||
| chr9:109498233-109498417 | Rare:62 | ||||
| chr9:110048373-110048796 | Common:3; Rare:127; Clinvar (benign):1 | ||||
| chr9:110125345-110125578 | Rare:45 |