| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:85741865-85742172 | Common:5; Rare:118 | ||||
| chr9:85940852-85941315 | Common:3; Rare:142 | ||||
| chr9:86354226-86354650 | Common:1; Rare:166 | ||||
| chr9:88388214-88388491 | Common:1; Rare:121 | ||||
| chr9:89310910-89311220 | Common:3; Rare:98 | ||||
| chr9:89318401-89318555 | Common:4; Rare:73 | ||||
| chr9:90801651-90801982 | Common:2; Rare:89 | ||||
| chr9:92115314-92115509 | Common:1; Rare:63; Clinvar:2 | ||||
| chr9:92293618-92293892 | Common:5; Rare:89 | ||||
| chr9:92325299-92326001 | Common:9; Rare:191 | ||||
| chr9:92404549-92404719 | Rare:38 | ||||
| chr9:92482475-92482822 | Rare:47 | ||||
| chr9:92535978-92536001 | Rare:2 | ||||
| chr9:92669990-92670375 | Common:1; Rare:122 | ||||
| chr9:92764683-92765006 | Common:1; Rare:108; Clinvar:1; Clinvar (benign):2 |