| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:108933940-108934537 | Common:9; Rare:235; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:109013383-109013713 | Common:2; Rare:126 | ||||
| chr9:110048518-110048844 | Common:3; Rare:118; Clinvar (benign):1 | ||||
| chr9:110256414-110256639 | Common:2; Rare:89 | ||||
| chr9:110256836-110256954 | Rare:25 | ||||
| chr9:111631132-111631398 | Common:1; Rare:75 | ||||
| chr9:111661533-111661691 | Common:2; Rare:51 | ||||
| chr9:111896621-111896814 | Common:3; Rare:79 | ||||
| chr9:112379793-112380161 | Common:4; Rare:144 | ||||
| chr9:112486669-112486975 | Rare:99 | ||||
| chr9:112750563-112750828 | Common:1; Rare:108 | ||||
| chr9:113056704-113056861 | Rare:48 | ||||
| chr9:113150644-113151019 | Common:5; Rare:82 | ||||
| chr9:113221227-113221620 | Common:1; Rare:125 | ||||
| chr9:113275363-113275734 | Common:5; Rare:116; Clinvar (pathogenic):1 |