| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:38137087-38137439 | Common:1; Rare:78 | ||||
| chr3:38165462-38165865 | Common:1; Rare:140 | ||||
| chr3:39051965-39052072 | Common:1; Rare:39 | ||||
| chr3:39107181-39107472 | Common:4; Rare:63 | ||||
| chr3:39107494-39107748 | Common:4; Rare:85 | ||||
| chr3:39107841-39107920 | Common:1; Rare:32 | ||||
| chr3:39153543-39153843 | Common:5; Rare:93 | ||||
| chr3:39383272-39383442 | Common:2; Rare:29; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:39383554-39383660 | Rare:26; Clinvar:2 | ||||
| chr3:39406921-39407160 | Common:5; Rare:90 | ||||
| chr3:40309448-40309835 | Common:9; Rare:134 | ||||
| chr3:40457204-40457389 | Common:3; Rare:92 | ||||
| chr3:40477051-40477184 | Common:1; Rare:34 | ||||
| chr3:40524852-40525013 | Rare:46 | ||||
| chr3:41199393-41199723 | Common:2; Rare:112 |