| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:54801180-54801540 | Common:2; Rare:71 | ||||
| chr1:54886510-54886862 | Common:1; Rare:182 | ||||
| chr1:54887108-54887622 | Common:6; Rare:341; Clinvar:12; Clinvar (benign):3 | ||||
| chr1:55039210-55039690 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
| chr1:55215060-55215711 | Common:2; Rare:341 | ||||
| chr1:56516988-56517129 | Common:2; Rare:39 | ||||
| chr1:56579262-56579511 | Common:1; Rare:65 | ||||
| chr1:56579540-56579700 | Rare:35 | ||||
| chr1:56819080-56819314 | Common:1; Rare:57 | ||||
| chr1:58546172-58546410 | Common:5; Rare:76 | ||||
| chr1:58546546-58546819 | Common:12; Rare:200 | ||||
| chr1:58577027-58577593 | Common:6; Rare:310; Clinvar:12; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr1:58699985-58700228 | Common:8; Rare:204 | ||||
| chr1:58783744-58784452 | Common:7; Rare:482 | ||||
| chr1:58784456-58784856 | Common:6; Rare:198 |