| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:137219323-137219487 | Common:2; Rare:56; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr6:138773642-138773795 | Common:1; Rare:69 | ||||
| chr6:139028576-139028832 | Common:1; Rare:52 | ||||
| chr6:143060700-143060935 | Common:7; Rare:82 | ||||
| chr6:143450654-143450929 | Common:1; Rare:103; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143677803-143678067 | Common:2; Rare:68 | ||||
| chr6:145814690-145814921 | Common:1; Rare:109 | ||||
| chr6:149749636-149749796 | Rare:89 | ||||
| chr6:151452049-151452548 | Common:4; Rare:179 | ||||
| chr6:152983022-152983315 | Common:2; Rare:93 | ||||
| chr6:153002627-153002838 | Common:3; Rare:80 | ||||
| chr6:157323497-157323597 | Common:2; Rare:37 | ||||
| chr6:158168210-158168378 | Common:2; Rare:57 | ||||
| chr6:158644710-158644914 | Common:2; Rare:79 | ||||
| chr6:158818226-158818385 | Common:3; Rare:63 |