| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36036800-36036986 | Common:2; Rare:62 | ||||
| chr9:36190737-36190994 | Common:1; Rare:86 | ||||
| chr9:36258386-36258625 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572770-36572902 | Rare:34 | ||||
| chr9:37422629-37422735 | Common:2; Rare:59 | ||||
| chr9:37800733-37800837 | Rare:29 | ||||
| chr9:37903899-37904463 | Common:4; Rare:188 | ||||
| chr9:43127044-43127447 | Common:2; Rare:110 | ||||
| chr9:66900548-66900804 | Common:3; Rare:81 | ||||
| chr9:68356380-68356619 | Common:7; Rare:41 | ||||
| chr9:69173883-69174193 | Common:5; Rare:95 | ||||
| chr9:69759904-69760147 | Common:3; Rare:103 | ||||
| chr9:70258833-70259075 | Common:4; Rare:113 | ||||
| chr9:70413930-70414192 | Rare:53 | ||||
| chr9:70414305-70414511 | Rare:48 |