| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:241640272-241640615 | Common:7; Rare:121 | ||||
| chr1:241847785-241847893 | Rare:38 | ||||
| chr1:241847907-241847996 | Common:1; Rare:19 | ||||
| chr1:241848000-241848261 | Common:4; Rare:64 | ||||
| chr1:243253427-243253465 | Rare:9 | ||||
| chr1:243254375-243254480 | Rare:21 | ||||
| chr1:243254649-243254986 | Common:2; Rare:99 | ||||
| chr1:243255005-243255395 | Common:1; Rare:93 | ||||
| chr1:243255716-243256198 | Common:1; Rare:148; Clinvar:5; Clinvar (benign):1 | ||||
| chr1:243256251-243256295 | Common:1; Rare:18 | ||||
| chr1:243269523-243269649 | Common:1; Rare:23 | ||||
| chr1:243850284-243850419 | Common:1; Rare:43 | ||||
| chr1:243850702-243850941 | Rare:76 | ||||
| chr1:243850989-243851183 | Rare:74 | ||||
| chr1:244451755-244452041 | Rare:90 |