| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906574-99906694 | Rare:62 | ||||
| chr9:100098966-100099363 | Common:4; Rare:118; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352846-100353103 | Rare:95 | ||||
| chr9:101398540-101398906 | Common:1; Rare:134 | ||||
| chr9:104093985-104094339 | Common:3; Rare:86 | ||||
| chr9:104094431-104094603 | Common:2; Rare:46 | ||||
| chr9:104747535-104747802 | Common:1; Rare:80 | ||||
| chr9:104764057-104764207 | Common:2; Rare:33 | ||||
| chr9:104927934-104927990 | Rare:14; Clinvar:4 | ||||
| chr9:105244511-105244838 | Common:3; Rare:115 | ||||
| chr9:105447936-105448153 | Common:2; Rare:82 | ||||
| chr9:105558067-105558148 | Rare:22 | ||||
| chr9:106862906-106863172 | Rare:80 | ||||
| chr9:107283450-107283639 | Common:3; Rare:42 | ||||
| chr9:107488439-107488645 | Common:1; Rare:56 |