| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100352831-100353114 | Rare:104 | ||||
| chr9:100426614-100426747 | Common:1; Rare:21 | ||||
| chr9:100427034-100427384 | Common:7; Rare:127 | ||||
| chr9:100429401-100429641 | Rare:38 | ||||
| chr9:101398511-101398887 | Common:1; Rare:137 | ||||
| chr9:101533737-101533914 | Rare:58 | ||||
| chr9:104093984-104094321 | Common:3; Rare:78 | ||||
| chr9:104094385-104094604 | Common:5; Rare:56 | ||||
| chr9:104747427-104747763 | Rare:87 | ||||
| chr9:105447966-105448153 | Common:2; Rare:70 | ||||
| chr9:106862978-106863180 | Rare:69 | ||||
| chr9:107282951-107283289 | Common:3; Rare:117 | ||||
| chr9:108934052-108934505 | Common:7; Rare:181; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:109013471-109013760 | Common:2; Rare:99 | ||||
| chr9:109498246-109498375 | Rare:43 |