| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:25819803-25820013 | Common:4; Rare:66 | ||||
| chr1:25906392-25906593 | Rare:79 | ||||
| chr1:26432253-26432422 | Common:3; Rare:44; Clinvar:2; Clinvar (benign):1 | ||||
| chr1:26472276-26472523 | Common:4; Rare:77 | ||||
| chr1:27322020-27322318 | Common:1; Rare:106 | ||||
| chr1:28552871-28553105 | Common:2; Rare:86 | ||||
| chr1:28643024-28643191 | Rare:64 | ||||
| chr1:28736884-28737018 | Rare:47 | ||||
| chr1:31296739-31297062 | Common:4; Rare:104 | ||||
| chr1:31703846-31704055 | Common:2; Rare:44 | ||||
| chr1:32200513-32200685 | Rare:39 | ||||
| chr1:32205632-32205662 | Rare:9 | ||||
| chr1:32650989-32651304 | Common:1; Rare:126 | ||||
| chr1:32817289-32817636 | Rare:84; Clinvar:5 | ||||
| chr1:33080994-33081157 | Common:1; Rare:38 |