| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:151198334-151198753 | Common:2; Rare:133 | ||||
| chr1:151254624-151254785 | Rare:40 | ||||
| chr1:151282127-151282330 | Rare:55 | ||||
| chr1:151399413-151399587 | Common:1; Rare:52; Clinvar (pathogenic):1 | ||||
| chr1:151511199-151511494 | Common:4; Rare:69 | ||||
| chr1:151790461-151790837 | Common:2; Rare:84 | ||||
| chr1:151909396-151909705 | Common:4; Rare:110 | ||||
| chr1:153535912-153536153 | Common:2; Rare:54 | ||||
| chr1:153536219-153536302 | Common:1; Rare:11 | ||||
| chr1:153544982-153545211 | Common:1; Rare:40 | ||||
| chr1:153545756-153545862 | Rare:18 | ||||
| chr1:153608937-153609154 | Common:1; Rare:43 | ||||
| chr1:153612960-153613282 | Common:1; Rare:62 | ||||
| chr1:153616304-153616547 | Common:1; Rare:48 | ||||
| chr1:153628055-153628148 | Common:1; Rare:24 |