| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:9890818-9891291 | Rare:124 | ||||
| chr3:9916883-9917155 | Common:3; Rare:65 | ||||
| chr3:9933441-9934115 | Common:4; Rare:233; Clinvar:4; Clinvar (benign):1 | ||||
| chr3:9952333-9952542 | Rare:46 | ||||
| chr3:9986717-9986969 | Common:3; Rare:83 | ||||
| chr3:9987310-9987595 | Common:1; Rare:72 | ||||
| chr3:10026243-10026538 | Common:1; Rare:86 | ||||
| chr3:10026578-10026754 | Common:1; Rare:41 | ||||
| chr3:10115441-10115768 | Common:4; Rare:116 | ||||
| chr3:10115850-10116089 | Common:1; Rare:49 | ||||
| chr3:10141638-10142144 | Common:3; Rare:222; Clinvar:56; Clinvar (benign):48; Clinvar (pathogenic):8 | ||||
| chr3:10164787-10164936 | Common:1; Rare:51 | ||||
| chr3:10248190-10248607 | Common:5; Rare:139 | ||||
| chr3:10248663-10248761 | Common:1; Rare:32 | ||||
| chr3:10248807-10248868 | Common:1; Rare:10 |