| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161749703-161749826 | Rare:44 | ||||
| chr1:161766041-161766376 | Common:3; Rare:87 | ||||
| chr1:162497707-162497868 | Common:2; Rare:52 | ||||
| chr1:162561351-162561604 | Common:3; Rare:99 | ||||
| chr1:162790548-162790785 | Common:4; Rare:68 | ||||
| chr1:163321723-163322025 | Common:1; Rare:85 | ||||
| chr1:165768692-165768933 | Common:1; Rare:88; Clinvar:1 | ||||
| chr1:166839345-166839551 | Rare:58 | ||||
| chr1:167220620-167220918 | Common:1; Rare:77 | ||||
| chr1:167935937-167936338 | Common:2; Rare:118 | ||||
| chr1:167936553-167936974 | Common:1; Rare:148 | ||||
| chr1:168225901-168226077 | Common:2; Rare:62 | ||||
| chr1:169367776-169368256 | Common:3; Rare:89 | ||||
| chr1:169485626-169486169 | Common:4; Rare:163; Clinvar:6; Clinvar (benign):4 | ||||
| chr1:169794868-169795047 | Common:3; Rare:37 |