| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221904-99222365 | Common:2; Rare:184; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:99821685-99822000 | Rare:91 | ||||
| chr9:99906597-99906690 | Rare:49 | ||||
| chr9:100098970-100099337 | Common:4; Rare:103; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352831-100353089 | Rare:93 | ||||
| chr9:101398511-101398895 | Common:1; Rare:140 | ||||
| chr9:104747617-104747784 | Common:1; Rare:52 | ||||
| chr9:106862979-106863182 | Rare:69 | ||||
| chr9:106863466-106863648 | Common:1; Rare:33 | ||||
| chr9:107489767-107490034 | Common:3; Rare:111 | ||||
| chr9:108933951-108933985 | Common:1; Rare:12; Clinvar:3 | ||||
| chr9:108934074-108934477 | Common:7; Rare:161; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109498238-109498457 | Rare:69 | ||||
| chr9:110256418-110256718 | Common:4; Rare:105 | ||||
| chr9:110579385-110579436 | Rare:19 |