| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134374431-134374667 | Rare:72 | ||||
| chr3:134485386-134485772 | Rare:91 | ||||
| chr3:134485956-134486260 | Common:3; Rare:107 | ||||
| chr3:134494563-134494820 | Common:1; Rare:45 | ||||
| chr3:135965564-135965794 | Common:1; Rare:100 | ||||
| chr3:136196299-136196514 | Common:1; Rare:72 | ||||
| chr3:136196562-136196991 | Common:1; Rare:134 | ||||
| chr3:136250292-136250381 | Common:2; Rare:37; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:136752341-136752736 | Common:1; Rare:131 | ||||
| chr3:136819035-136819198 | Common:3; Rare:90 | ||||
| chr3:136862014-136862298 | Common:1; Rare:90 | ||||
| chr3:138115570-138115720 | Common:4; Rare:38 | ||||
| chr3:138174849-138174965 | Common:1; Rare:28 | ||||
| chr3:138187156-138187385 | Common:1; Rare:61 | ||||
| chr3:138594200-138594451 | Rare:74 |