| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:113376908-113377118 | Common:7; Rare:70 | ||||
| chr9:113401248-113401430 | Common:6; Rare:79; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410201-113410756 | Common:4; Rare:180 | ||||
| chr9:113463562-113463779 | Common:2; Rare:73 | ||||
| chr9:113565338-113565504 | Common:1; Rare:49 | ||||
| chr9:114505506-114505595 | Rare:25 | ||||
| chr9:114587554-114587910 | Common:3; Rare:142 | ||||
| chr9:116153565-116153866 | Common:1; Rare:70 | ||||
| chr9:116687171-116687364 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120402968-120403643 | Common:2; Rare:134; Clinvar:2 | ||||
| chr9:120580118-120580315 | Rare:59; Clinvar:5 | ||||
| chr9:120793242-120793575 | Common:5; Rare:118 | ||||
| chr9:120842881-120843258 | Common:1; Rare:124 | ||||
| chr9:120868841-120869026 | Common:1; Rare:38 | ||||
| chr9:120876375-120876595 | Common:2; Rare:64 |