| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38138596-38138701 | Common:2; Rare:43; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr3:39051956-39052042 | Common:1; Rare:31 | ||||
| chr3:39107597-39107680 | Common:2; Rare:26 | ||||
| chr3:39383283-39383415 | Rare:24; Clinvar:1 | ||||
| chr3:39383547-39383653 | Rare:25; Clinvar:1 | ||||
| chr3:39406596-39406763 | Common:2; Rare:70 | ||||
| chr3:40309471-40309808 | Common:9; Rare:115 | ||||
| chr3:40457201-40457388 | Common:3; Rare:91 | ||||
| chr3:40524795-40524960 | Common:1; Rare:41 | ||||
| chr3:41962045-41962333 | Common:4; Rare:70 | ||||
| chr3:42160071-42160212 | Common:1; Rare:32 | ||||
| chr3:42581917-42582156 | Common:3; Rare:73 | ||||
| chr3:42590651-42590958 | Common:3; Rare:94 | ||||
| chr3:42600320-42600749 | Common:3; Rare:169 | ||||
| chr3:42804427-42804679 | Common:2; Rare:79 |