| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:45340316-45340579 | Common:2; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:45491059-45491406 | Common:3; Rare:93 | ||||
| chr1:45499998-45500369 | Common:2; Rare:87; Clinvar:4; Clinvar (pathogenic):3 | ||||
| chr1:45521806-45522087 | Common:1; Rare:106 | ||||
| chr1:45550716-45551150 | Common:3; Rare:102 | ||||
| chr1:45568661-45568941 | Common:1; Rare:59 | ||||
| chr1:45583301-45583599 | Common:3; Rare:78 | ||||
| chr1:45583927-45584201 | Common:1; Rare:106 | ||||
| chr1:45608668-45608955 | Rare:47 | ||||
| chr1:45613131-45613186 | Common:1; Rare:15 | ||||
| chr1:45686996-45687351 | Common:2; Rare:90 | ||||
| chr1:45688042-45688253 | Common:1; Rare:58 | ||||
| chr1:45803505-45803655 | Common:1; Rare:57 | ||||
| chr1:46132624-46133237 | Common:3; Rare:181 | ||||
| chr1:46198329-46198593 | Common:5; Rare:126; Clinvar:1; Clinvar (benign):1 |