| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38164987-38165272 | Common:1; Rare:67 | ||||
| chr3:38165428-38165537 | Rare:31 | ||||
| chr3:38282192-38282338 | Rare:28 | ||||
| chr3:38496293-38496515 | Rare:121 | ||||
| chr3:39051917-39052306 | Common:3; Rare:119 | ||||
| chr3:39052438-39052561 | Rare:40 | ||||
| chr3:39107203-39107500 | Common:4; Rare:65 | ||||
| chr3:39107531-39107850 | Common:5; Rare:93 | ||||
| chr3:39153543-39153745 | Common:3; Rare:64 | ||||
| chr3:39383289-39383432 | Common:1; Rare:24; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:39383571-39383694 | Rare:27; Clinvar:1 | ||||
| chr3:39406614-39406991 | Common:4; Rare:144 | ||||
| chr3:39502287-39502376 | Common:1; Rare:33 | ||||
| chr3:40309446-40309960 | Common:9; Rare:173 | ||||
| chr3:40457201-40457381 | Common:3; Rare:86 |