| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128882947-128883211 | Common:1; Rare:56 | ||||
| chr9:128912443-128912807 | Common:2; Rare:61 | ||||
| chr9:128921976-128922344 | Common:2; Rare:86 | ||||
| chr9:128947573-128947735 | Common:1; Rare:73; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129080788-129081130 | Common:2; Rare:93 | ||||
| chr9:129110653-129111029 | Common:5; Rare:117 | ||||
| chr9:129111087-129111450 | Common:4; Rare:104 | ||||
| chr9:129835214-129835490 | Common:2; Rare:111 | ||||
| chr9:130043079-130043314 | Common:2; Rare:78 | ||||
| chr9:130053424-130053713 | Common:1; Rare:62 | ||||
| chr9:130053847-130054031 | Common:1; Rare:69 | ||||
| chr9:130579428-130579683 | Common:7; Rare:106 | ||||
| chr9:130693540-130693835 | Common:1; Rare:102 | ||||
| chr9:130713441-130713646 | Common:2; Rare:47 | ||||
| chr9:131096200-131096660 | Common:4; Rare:119 |