| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128191785-128191906 | Common:1; Rare:31 | ||||
| chr9:128275929-128276293 | Common:4; Rare:166 | ||||
| chr9:128322404-128322535 | Common:1; Rare:46 | ||||
| chr9:128322728-128322861 | Common:2; Rare:49; Clinvar (benign):5 | ||||
| chr9:128371220-128371383 | Rare:55 | ||||
| chr9:128455995-128456192 | Common:1; Rare:71 | ||||
| chr9:128552383-128552593 | Rare:74; Clinvar:1 | ||||
| chr9:128656662-128656767 | Common:1; Rare:54; Clinvar (pathogenic):1 | ||||
| chr9:128724089-128724467 | Common:2; Rare:125 | ||||
| chr9:128881916-128882186 | Common:1; Rare:90 | ||||
| chr9:128921987-128922314 | Common:1; Rare:75 | ||||
| chr9:128947599-128947738 | Common:1; Rare:65; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129110653-129110919 | Common:2; Rare:56 | ||||
| chr9:129139903-129140122 | Rare:43 | ||||
| chr9:129803056-129803194 | Common:2; Rare:42 |