| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101398503-101398910 | Common:1; Rare:145 | ||||
| chr9:104093985-104094327 | Common:3; Rare:80 | ||||
| chr9:104094494-104094627 | Common:2; Rare:43 | ||||
| chr9:104747559-104747795 | Common:1; Rare:70 | ||||
| chr9:104764057-104764193 | Common:2; Rare:30 | ||||
| chr9:104927941-104927990 | Rare:11; Clinvar:4 | ||||
| chr9:105558082-105558159 | Rare:20; Clinvar (benign):1 | ||||
| chr9:106862965-106863186 | Rare:76 | ||||
| chr9:107282981-107283307 | Common:1; Rare:108 | ||||
| chr9:107488202-107488582 | Common:2; Rare:114 | ||||
| chr9:107489767-107490063 | Common:4; Rare:128 | ||||
| chr9:108934065-108934489 | Common:7; Rare:168; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498278-109498423 | Rare:52 | ||||
| chr9:110125368-110125595 | Rare:48 | ||||
| chr9:110127351-110127490 | Rare:24 |