| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:88388800-88389320 | Common:2; Rare:200 | ||||
| chr9:88991329-88991479 | Common:1; Rare:41 | ||||
| chr9:89310749-89311213 | Common:6; Rare:155 | ||||
| chr9:89318405-89318511 | Common:3; Rare:46 | ||||
| chr9:89318661-89318902 | Rare:67 | ||||
| chr9:89604808-89605133 | Common:6; Rare:90 | ||||
| chr9:90642783-90643051 | Common:1; Rare:79 | ||||
| chr9:91361710-91362160 | Common:3; Rare:144; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:91423807-91424015 | Common:1; Rare:60 | ||||
| chr9:92114776-92115176 | Common:3; Rare:114 | ||||
| chr9:92115378-92115544 | Common:1; Rare:45; Clinvar:1 | ||||
| chr9:92293638-92293983 | Common:5; Rare:117 | ||||
| chr9:92325289-92325999 | Common:9; Rare:192 | ||||
| chr9:92670076-92670406 | Common:1; Rare:105 | ||||
| chr9:92764830-92765222 | Common:2; Rare:121 |