| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:161226742-161226942 | Rare:46 | ||||
| chr1:161227476-161227645 | Rare:32 | ||||
| chr1:161258605-161258763 | Common:1; Rare:33 | ||||
| chr1:161306124-161306328 | Common:1; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr1:161314196-161314474 | Common:4; Rare:108; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr1:161314846-161315089 | Common:1; Rare:51 | ||||
| chr1:161523918-161524247 | Common:9; Rare:97 | ||||
| chr1:161524358-161524546 | Common:3; Rare:63 | ||||
| chr1:161706776-161706987 | Common:1; Rare:37 | ||||
| chr1:161707019-161707304 | Common:3; Rare:73 | ||||
| chr1:161726180-161726331 | Common:1; Rare:49 | ||||
| chr1:161726357-161726646 | Common:1; Rare:85 | ||||
| chr1:161749614-161749949 | Rare:121 | ||||
| chr1:161750179-161750351 | Rare:47 | ||||
| chr1:161766129-161766385 | Common:3; Rare:80 |