| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113275354-113275746 | Common:5; Rare:128; Clinvar (pathogenic):1 | ||||
| chr9:113340237-113340341 | Common:2; Rare:28 | ||||
| chr9:113376873-113377118 | Common:8; Rare:78 | ||||
| chr9:113410281-113410776 | Common:4; Rare:158 | ||||
| chr9:114387967-114388166 | Common:1; Rare:57 | ||||
| chr9:114930278-114930432 | Rare:39 | ||||
| chr9:116687228-116687361 | Common:1; Rare:43; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120532519-120532738 | Rare:43 | ||||
| chr9:120533027-120533202 | Rare:35 | ||||
| chr9:120714452-120714715 | Common:2; Rare:87 | ||||
| chr9:120793242-120793564 | Common:5; Rare:115 | ||||
| chr9:120842897-120843272 | Common:1; Rare:123 | ||||
| chr9:120843314-120843509 | Common:2; Rare:44 | ||||
| chr9:120868827-120869127 | Common:2; Rare:67 | ||||
| chr9:120877147-120877466 | Common:3; Rare:102 |