| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:112333539-112333944 | Rare:126 | ||||
| chr9:112379762-112380157 | Common:4; Rare:150 | ||||
| chr9:113056674-113056909 | Rare:77 | ||||
| chr9:113188006-113188145 | Common:2; Rare:18 | ||||
| chr9:113221242-113221619 | Common:1; Rare:118 | ||||
| chr9:113275354-113275735 | Common:5; Rare:123; Clinvar (pathogenic):1 | ||||
| chr9:113401242-113401488 | Common:6; Rare:96; Clinvar:5; Clinvar (benign):3 | ||||
| chr9:113410286-113410741 | Common:4; Rare:143 | ||||
| chr9:113517074-113517325 | Common:1; Rare:55 | ||||
| chr9:113593848-113594156 | Common:4; Rare:118 | ||||
| chr9:114587554-114587868 | Common:3; Rare:126 | ||||
| chr9:115118061-115118114 | Common:2; Rare:13 | ||||
| chr9:115118140-115118563 | Common:1; Rare:87 | ||||
| chr9:116687171-116687364 | Common:4; Rare:74; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:120580118-120580315 | Rare:59; Clinvar:5 |