| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151254627-151254803 | Rare:46 | ||||
| chr1:151281946-151282337 | Rare:114 | ||||
| chr1:151346852-151347037 | Rare:52 | ||||
| chr1:151399480-151399596 | Common:1; Rare:40; Clinvar (pathogenic):1 | ||||
| chr1:151511150-151511476 | Common:4; Rare:72 | ||||
| chr1:151540136-151540373 | Common:1; Rare:79 | ||||
| chr1:151763423-151763557 | Common:2; Rare:52 | ||||
| chr1:151790419-151790869 | Common:3; Rare:108 | ||||
| chr1:151993751-151993959 | Common:4; Rare:75 | ||||
| chr1:153535924-153536153 | Common:1; Rare:52 | ||||
| chr1:153565668-153565993 | Common:2; Rare:53 | ||||
| chr1:153608066-153608267 | Rare:64 | ||||
| chr1:153608916-153609143 | Common:1; Rare:43 | ||||
| chr1:153609344-153609417 | Common:2; Rare:14 | ||||
| chr1:153633862-153634132 | Common:4; Rare:81 |