| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:105244228-105244724 | Common:8; Rare:282 | ||||
| chr9:105447800-105448180 | Common:8; Rare:192 | ||||
| chr9:105558067-105558192 | Rare:62; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:107282889-107283370 | Common:6; Rare:280 | ||||
| chr9:107283412-107283669 | Common:6; Rare:116 | ||||
| chr9:107283890-107284270 | Common:4; Rare:117 | ||||
| chr9:107489749-107490034 | Common:6; Rare:229 | ||||
| chr9:107490180-107490630 | Common:2; Rare:141 | ||||
| chr9:108933896-108934528 | Common:19; Rare:471; Clinvar:14; Clinvar (benign):6 | ||||
| chr9:109119909-109120270 | Common:28; Rare:210 | ||||
| chr9:109320960-109321380 | Common:1; Rare:126 | ||||
| chr9:109498246-109498379 | Rare:44 | ||||
| chr9:110256414-110256729 | Common:9; Rare:215 | ||||
| chr9:111483506-111483648 | Common:2; Rare:61 | ||||
| chr9:111483804-111484075 | Rare:104 |