| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161197210-161197419 | Common:2; Rare:36 | ||||
| chr1:161199028-161199304 | Rare:43 | ||||
| chr1:161215172-161215330 | Common:2; Rare:51 | ||||
| chr1:161505276-161505476 | Common:1; Rare:36 | ||||
| chr1:161766198-161766365 | Common:3; Rare:56 | ||||
| chr1:162023343-162023575 | Common:3; Rare:65; Clinvar (pathogenic):1 | ||||
| chr1:162023617-162023921 | Common:1; Rare:84 | ||||
| chr1:162790553-162790781 | Common:4; Rare:64 | ||||
| chr1:163202888-163203226 | Common:1; Rare:62 | ||||
| chr1:163321706-163322066 | Common:1; Rare:97 | ||||
| chr1:164558795-164559072 | Rare:77 | ||||
| chr1:164559321-164559529 | Rare:58 | ||||
| chr1:164559596-164559785 | Common:2; Rare:43 | ||||
| chr1:165631128-165631284 | Common:4; Rare:44 | ||||
| chr1:165698482-165698634 | Common:2; Rare:87 |