| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35814975-35815293 | Rare:80 | ||||
| chr9:36190737-36190994 | Common:1; Rare:86 | ||||
| chr9:36258395-36258625 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37904066-37904462 | Common:3; Rare:131 | ||||
| chr9:69759930-69760143 | Common:3; Rare:95 | ||||
| chr9:70258839-70259069 | Common:4; Rare:107 | ||||
| chr9:75088093-75088570 | Common:4; Rare:166 | ||||
| chr9:78296871-78297217 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr9:83707677-83708300 | Common:5; Rare:203 | ||||
| chr9:83921402-83921657 | Common:2; Rare:107 | ||||
| chr9:83956654-83956809 | Common:2; Rare:45 | ||||
| chr9:83980164-83980435 | Rare:103 | ||||
| chr9:83980530-83980844 | Common:5; Rare:132 | ||||
| chr9:86354369-86354578 | Rare:72 | ||||
| chr9:87726005-87726263 | Common:4; Rare:77 |