| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:154220348-154220380 | Rare:6 | ||||
| chr1:154220498-154220973 | Common:1; Rare:161 | ||||
| chr1:154272462-154272773 | Common:4; Rare:81; Clinvar:3; Clinvar (benign):3 | ||||
| chr1:154627889-154628039 | Common:3; Rare:79 | ||||
| chr1:154936618-154936795 | Common:3; Rare:59 | ||||
| chr1:154956073-154956253 | Common:1; Rare:52 | ||||
| chr1:154966203-154966440 | Common:1; Rare:74 | ||||
| chr1:154970031-154970509 | Common:1; Rare:149 | ||||
| chr1:154970699-154970986 | Common:1; Rare:60 | ||||
| chr1:154974322-154974738 | Rare:108 | ||||
| chr1:154983102-154983393 | Common:2; Rare:57; Clinvar (benign):1 | ||||
| chr1:155002384-155002686 | Common:2; Rare:28 | ||||
| chr1:155051118-155051373 | Common:2; Rare:87 | ||||
| chr1:155127213-155127483 | Common:2; Rare:52 | ||||
| chr1:155127673-155127962 | Common:1; Rare:67 |