| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151399452-151399805 | Common:4; Rare:112; Clinvar (pathogenic):2 | ||||
| chr1:151540275-151540445 | Common:2; Rare:69 | ||||
| chr1:151562453-151562681 | Common:1; Rare:55 | ||||
| chr1:151565850-151565950 | Common:2; Rare:26 | ||||
| chr1:151763360-151763550 | Common:2; Rare:80 | ||||
| chr1:151790411-151790874 | Common:3; Rare:113 | ||||
| chr1:151992569-151992820 | Common:1; Rare:57 | ||||
| chr1:151993747-151994284 | Common:6; Rare:153 | ||||
| chr1:152036909-152037050 | Common:1; Rare:39 | ||||
| chr1:152037055-152037095 | Rare:10 | ||||
| chr1:152325210-152325317 | Common:1; Rare:13 | ||||
| chr1:152414261-152414586 | Common:2; Rare:64 | ||||
| chr1:152514369-152514552 | Common:2; Rare:34 | ||||
| chr1:152804894-152805055 | Common:1; Rare:28 | ||||
| chr1:152970360-152970653 | Common:2; Rare:48 |