| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134485356-134485772 | Rare:95 | ||||
| chr3:134485950-134486317 | Common:4; Rare:128 | ||||
| chr3:135965553-135965844 | Common:1; Rare:116 | ||||
| chr3:136196562-136196737 | Rare:50 | ||||
| chr3:136196843-136196993 | Common:1; Rare:47 | ||||
| chr3:136250281-136250381 | Common:2; Rare:40; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:136752229-136752873 | Common:1; Rare:223 | ||||
| chr3:136818293-136818505 | Rare:32 | ||||
| chr3:136819018-136819221 | Common:4; Rare:100 | ||||
| chr3:136862014-136862319 | Common:1; Rare:97 | ||||
| chr3:138115564-138115722 | Common:4; Rare:40 | ||||
| chr3:138174822-138174960 | Common:2; Rare:35 | ||||
| chr3:138594170-138594521 | Rare:112 | ||||
| chr3:138608541-138608629 | Rare:24 | ||||
| chr3:138608637-138608891 | Rare:51 |