| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45326800-45326917 | Rare:26 | ||||
| chr1:45339959-45340243 | Rare:103; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr1:45340388-45340470 | Common:1; Rare:21; Clinvar:1 | ||||
| chr1:45500056-45500359 | Common:1; Rare:74; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521817-45522089 | Common:1; Rare:102 | ||||
| chr1:45550721-45551099 | Common:3; Rare:92 | ||||
| chr1:45583940-45584170 | Rare:89 | ||||
| chr1:45687059-45687353 | Common:1; Rare:77 | ||||
| chr1:45688055-45688247 | Common:1; Rare:55 | ||||
| chr1:45750622-45750793 | Rare:63 | ||||
| chr1:46198389-46198517 | Common:1; Rare:51; Clinvar:1 | ||||
| chr1:46303138-46303303 | Common:1; Rare:57 | ||||
| chr1:46303308-46303763 | Common:2; Rare:124 | ||||
| chr1:46340664-46340819 | Common:3; Rare:39 | ||||
| chr1:47314088-47314448 | Common:3; Rare:76; Clinvar:1 |