| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:150560836-150561136 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):2 | ||||
| chr1:150561245-150561641 | Common:3; Rare:272 | ||||
| chr1:150561988-150562375 | Common:2; Rare:203 | ||||
| chr1:150568100-150568610 | Rare:233 | ||||
| chr1:150577139-150577882 | Common:8; Rare:236; Clinvar:1 | ||||
| chr1:150585792-150586601 | Common:8; Rare:259 | ||||
| chr1:150619861-150620378 | Common:6; Rare:216 | ||||
| chr1:150906266-150906666 | Common:3; Rare:68 | ||||
| chr1:150952273-150953106 | Common:2; Rare:265 | ||||
| chr1:150954483-150955001 | Common:3; Rare:122 | ||||
| chr1:150958482-150959622 | Common:12; Rare:528 | ||||
| chr1:150960143-150960773 | Common:3; Rare:150 | ||||
| chr1:150966153-150967102 | Common:10; Rare:425 | ||||
| chr1:150972659-150972778 | Rare:21 | ||||
| chr1:150977276-150977686 | Common:6; Rare:203 |