| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1353826-1354109 | Common:1; Rare:143; Clinvar (pathogenic):1 | ||||
| chr1:1358513-1358739 | Common:1; Rare:83 | ||||
| chr1:1358741-1358979 | Common:2; Rare:59 | ||||
| chr1:1375246-1375615 | Common:7; Rare:110 | ||||
| chr1:1399306-1399597 | Common:1; Rare:128 | ||||
| chr1:1406970-1407409 | Common:2; Rare:195 | ||||
| chr1:1435551-1435756 | Rare:75 | ||||
| chr1:1477667-1477863 | Common:3; Rare:40 | ||||
| chr1:1574490-1574963 | Common:1; Rare:202 | ||||
| chr1:1615200-1615584 | Common:4; Rare:166 | ||||
| chr1:1632044-1632207 | Common:2; Rare:54 | ||||
| chr1:1658889-1659089 | Common:4; Rare:81 | ||||
| chr1:1724233-1724504 | Common:4; Rare:94 | ||||
| chr1:1889863-1890048 | Rare:46 | ||||
| chr1:2194010-2194379 | Common:1; Rare:111 |