| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:207321092-207321233 | Common:1; Rare:27 | ||||
| chr1:207321364-207321766 | Common:2; Rare:96 | ||||
| chr1:207751885-207752175 | Common:1; Rare:97 | ||||
| chr1:207752290-207752403 | Rare:34 | ||||
| chr1:209583507-209583763 | Rare:54 | ||||
| chr1:209584181-209584339 | Rare:37 | ||||
| chr1:209675275-209675418 | Common:1; Rare:38 | ||||
| chr1:209768959-209769012 | Rare:8 | ||||
| chr1:209784111-209784311 | Rare:31 | ||||
| chr1:209784443-209784869 | Common:4; Rare:126 | ||||
| chr1:209806160-209806383 | Common:4; Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr1:209827742-209828076 | Common:4; Rare:86 | ||||
| chr1:209828303-209828423 | Common:1; Rare:17 | ||||
| chr1:209937952-209938328 | Common:3; Rare:138; Clinvar (pathogenic):1 | ||||
| chr1:209938470-209938532 | Rare:22 |