| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:145918686-145919027 | Common:2; Rare:75 | ||||
| chr1:145927422-145927644 | Common:1; Rare:65; Clinvar (pathogenic):1 | ||||
| chr1:145958007-145958223 | Rare:52 | ||||
| chr1:145964558-145964759 | Rare:49 | ||||
| chr1:145994927-145995477 | Rare:230 | ||||
| chr1:145996348-145996906 | Common:2; Rare:194 | ||||
| chr1:146228968-146229182 | Common:2; Rare:46 | ||||
| chr1:146938261-146938331 | Rare:26 | ||||
| chr1:147172420-147172830 | Common:1; Rare:105 | ||||
| chr1:147541222-147541572 | Common:2; Rare:55 | ||||
| chr1:147928274-147928448 | Common:2; Rare:59 | ||||
| chr1:148889401-148889893 | Common:2; Rare:127 | ||||
| chr1:148952242-148952623 | Common:5; Rare:103 | ||||
| chr1:149812158-149812532 | Common:2; Rare:168 | ||||
| chr1:149842746-149842947 | Rare:3 |