| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:36088741-36088922 | Common:1; Rare:67 | ||||
| chr1:36397881-36398008 | Common:2; Rare:30 | ||||
| chr1:36464180-36464467 | Common:2; Rare:87 | ||||
| chr1:37474395-37474581 | Common:1; Rare:74 | ||||
| chr1:37690502-37690653 | Common:3; Rare:44 | ||||
| chr1:37692215-37692577 | Common:4; Rare:85 | ||||
| chr1:37859594-37859764 | Common:3; Rare:56 | ||||
| chr1:38873281-38873554 | Common:3; Rare:89 | ||||
| chr1:39026245-39026396 | Common:1; Rare:40 | ||||
| chr1:39738746-39738907 | Common:2; Rare:33 | ||||
| chr1:39883454-39883570 | Common:1; Rare:48; Clinvar (pathogenic):1 | ||||
| chr1:39954919-39955165 | Common:1; Rare:63 | ||||
| chr1:40040444-40040830 | Common:3; Rare:117 | ||||
| chr1:40161234-40161394 | Common:1; Rare:42 | ||||
| chr1:40257908-40258282 | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 |