| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:179294544-179294715 | Rare:26 | ||||
| chr1:179365663-179365818 | Common:5; Rare:40 | ||||
| chr1:179365867-179366180 | Common:10; Rare:67 | ||||
| chr1:179366187-179366315 | Common:2; Rare:25 | ||||
| chr1:179366429-179366472 | Rare:8 | ||||
| chr1:179551400-179551585 | Common:2; Rare:42; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr1:179877741-179877945 | Rare:42 | ||||
| chr1:179881429-179881673 | Rare:44 | ||||
| chr1:179883778-179884005 | Common:2; Rare:42 | ||||
| chr1:179954281-179954915 | Common:3; Rare:144 | ||||
| chr1:179955099-179955305 | Common:1; Rare:42 | ||||
| chr1:180154398-180154511 | Common:2; Rare:37 | ||||
| chr1:180154557-180155055 | Common:6; Rare:157 | ||||
| chr1:180229862-180229950 | Rare:32 | ||||
| chr1:180502272-180503228 | Common:3; Rare:328 |