| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:145858917-145859317 | Rare:382 | ||||
| chr1:145859660-145860089 | Common:9; Rare:260 | ||||
| chr1:145918658-145919133 | Common:10; Rare:441; Clinvar:4 | ||||
| chr1:145927353-145927753 | Common:3; Rare:412; Clinvar (pathogenic):3 | ||||
| chr1:145957239-145957636 | Rare:162 | ||||
| chr1:145957540-145958324 | Common:4; Rare:667 | ||||
| chr1:145962058-145962893 | Common:7; Rare:193 | ||||
| chr1:145964074-145965088 | Rare:484 | ||||
| chr1:145993346-145995952 | Common:7; Rare:2063 | ||||
| chr1:145996136-145996276 | Rare:110 | ||||
| chr1:145996351-145996930 | Common:7; Rare:817 | ||||
| chr1:146021037-146021437 | Common:1; Rare:63 | ||||
| chr1:146021590-146022010 | Rare:209; Clinvar:4 | ||||
| chr1:146937659-146938540 | Common:5; Rare:297 | ||||
| chr1:147172132-147173153 | Common:12; Rare:786 |