| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36190737-36190966 | Common:1; Rare:78 | ||||
| chr9:36572801-36572927 | Rare:31 | ||||
| chr9:37120354-37120592 | Common:2; Rare:84 | ||||
| chr9:37485737-37486047 | Common:3; Rare:112 | ||||
| chr9:37904079-37904241 | Common:2; Rare:50 | ||||
| chr9:69759930-69760080 | Common:2; Rare:76 | ||||
| chr9:70258824-70259047 | Common:4; Rare:109 | ||||
| chr9:75088177-75088563 | Common:3; Rare:140 | ||||
| chr9:78296831-78297228 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr9:83707683-83708267 | Common:5; Rare:187 | ||||
| chr9:83979609-83979743 | Rare:42 | ||||
| chr9:83980146-83980369 | Common:1; Rare:81 | ||||
| chr9:83980556-83980834 | Common:5; Rare:120 | ||||
| chr9:86282516-86282692 | Common:2; Rare:81 | ||||
| chr9:86354372-86354581 | Rare:73 |