| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:83707914-83708015 | Rare:39 | ||||
| chr9:83980562-83980803 | Common:3; Rare:99 | ||||
| chr9:88388214-88388466 | Common:1; Rare:107 | ||||
| chr9:89310959-89311205 | Common:2; Rare:68 | ||||
| chr9:92325334-92325662 | Common:5; Rare:76 | ||||
| chr9:97633535-97633821 | Common:4; Rare:87 | ||||
| chr9:99221964-99222349 | Common:2; Rare:139 | ||||
| chr9:99906607-99906684 | Rare:35 | ||||
| chr9:100098979-100099314 | Common:2; Rare:92; Clinvar:2 | ||||
| chr9:100352887-100353033 | Rare:41 | ||||
| chr9:101398591-101398887 | Common:1; Rare:96 | ||||
| chr9:113221286-113221607 | Rare:98 | ||||
| chr9:113275403-113275708 | Common:5; Rare:97; Clinvar (pathogenic):1 | ||||
| chr9:120793359-120793527 | Common:1; Rare:65 | ||||
| chr9:121201850-121202139 | Common:2; Rare:80 |