| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37785021-37785149 | Common:1; Rare:57; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:37800733-37800837 | Rare:29 | ||||
| chr9:37904046-37904229 | Rare:60 | ||||
| chr9:37904308-37904476 | Rare:62 | ||||
| chr9:38392536-38392806 | Common:2; Rare:77 | ||||
| chr9:43127129-43127441 | Common:2; Rare:81 | ||||
| chr9:66900559-66900811 | Common:3; Rare:80 | ||||
| chr9:68356354-68356635 | Common:7; Rare:49 | ||||
| chr9:68356657-68356806 | Common:1; Rare:39 | ||||
| chr9:68356836-68357221 | Common:6; Rare:118 | ||||
| chr9:68357224-68357386 | Rare:43 | ||||
| chr9:69759930-69760123 | Common:2; Rare:88 | ||||
| chr9:70043717-70043877 | Rare:30 | ||||
| chr9:70043890-70044221 | Common:2; Rare:65 | ||||
| chr9:70258833-70259071 | Common:4; Rare:112 |