| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:32200551-32200677 | Rare:31 | ||||
| chr1:32222323-32222589 | Rare:103 | ||||
| chr1:32394411-32394657 | Common:1; Rare:66 | ||||
| chr1:32650926-32651318 | Common:2; Rare:149 | ||||
| chr1:32817289-32817636 | Rare:84; Clinvar:5 | ||||
| chr1:33021451-33021656 | Rare:47; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr1:34985301-34985380 | Common:1; Rare:28 | ||||
| chr1:35079347-35079422 | Common:3; Rare:25 | ||||
| chr1:35557345-35557451 | Rare:31 | ||||
| chr1:35557636-35557850 | Common:2; Rare:86 | ||||
| chr1:36149439-36149803 | Common:2; Rare:99 | ||||
| chr1:36155854-36156180 | Rare:124 | ||||
| chr1:36178123-36178735 | Common:2; Rare:181 | ||||
| chr1:36450419-36450595 | Common:1; Rare:54 | ||||
| chr1:36464146-36464492 | Common:2; Rare:112 |