| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99103843-99104036 | Rare:24 | ||||
| chr9:99221927-99222357 | Common:2; Rare:163; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99821610-99821893 | Rare:94 | ||||
| chr9:99906591-99906690 | Rare:49 | ||||
| chr9:100098974-100099334 | Common:3; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352841-100353071 | Rare:79 | ||||
| chr9:101398580-101398998 | Common:1; Rare:124 | ||||
| chr9:105558009-105558153 | Rare:48 | ||||
| chr9:106862873-106863180 | Rare:87 | ||||
| chr9:107489767-107490063 | Common:4; Rare:128 | ||||
| chr9:108934074-108934477 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498253-109498457 | Rare:65 | ||||
| chr9:110256431-110256693 | Common:3; Rare:98 | ||||
| chr9:110579147-110579285 | Rare:43 | ||||
| chr9:110579868-110579990 | Common:1; Rare:38 |