| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128190439-128190720 | Rare:115 | ||||
| chr9:128191453-128191723 | Common:1; Rare:133 | ||||
| chr9:128191731-128192320 | Common:2; Rare:154 | ||||
| chr9:128250301-128250762 | Rare:185; Clinvar (benign):3 | ||||
| chr9:128275522-128275922 | Common:2; Rare:140 | ||||
| chr9:128275896-128276350 | Common:10; Rare:394 | ||||
| chr9:128322121-128322651 | Common:4; Rare:282 | ||||
| chr9:128322718-128323064 | Common:6; Rare:256; Clinvar:7; Clinvar (benign):17; Clinvar (pathogenic):4 | ||||
| chr9:128340416-128340759 | Common:4; Rare:209 | ||||
| chr9:128371146-128371455 | Common:1; Rare:195 | ||||
| chr9:128455924-128456246 | Common:3; Rare:184 | ||||
| chr9:128456280-128456470 | Common:1; Rare:52 | ||||
| chr9:128504569-128504850 | Rare:236; Clinvar:12 | ||||
| chr9:128552339-128552697 | Common:1; Rare:226; Clinvar:8; Clinvar (benign):4 | ||||
| chr9:128636238-128636677 | Common:4; Rare:123; Clinvar (benign):2 |