| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37690495-37690737 | Common:5; Rare:61 | ||||
| chr1:37692204-37692589 | Common:5; Rare:90 | ||||
| chr1:37859569-37859814 | Common:4; Rare:86 | ||||
| chr1:37946992-37947114 | Rare:24 | ||||
| chr1:37989961-37990133 | Rare:68 | ||||
| chr1:38005491-38005759 | Common:1; Rare:67 | ||||
| chr1:38012539-38012823 | Rare:88 | ||||
| chr1:38873301-38873595 | Common:4; Rare:103 | ||||
| chr1:39026243-39026398 | Common:1; Rare:41 | ||||
| chr1:39204575-39204868 | Rare:49 | ||||
| chr1:39883447-39883590 | Common:1; Rare:59; Clinvar (pathogenic):1 | ||||
| chr1:40039884-40040248 | Common:3; Rare:77 | ||||
| chr1:40040439-40040806 | Common:3; Rare:112 | ||||
| chr1:40161231-40161405 | Common:1; Rare:48 | ||||
| chr1:40257908-40258282 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 |