| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151493938-151494135 | Common:2; Rare:104 | ||||
| chr6:152302000-152302380 | Common:1; Rare:156; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152381273-152381429 | Rare:45; Clinvar:5; Clinvar (pathogenic):1 | ||||
| chr6:152983017-152983383 | Common:4; Rare:216 | ||||
| chr6:152983494-152983783 | Common:8; Rare:205 | ||||
| chr6:153002666-153002976 | Common:8; Rare:175 | ||||
| chr6:154510200-154510430 | Common:1; Rare:78 | ||||
| chr6:154510480-154510877 | Common:8; Rare:234 | ||||
| chr6:154733195-154733512 | Rare:211 | ||||
| chr6:154733532-154733756 | Common:3; Rare:92 | ||||
| chr6:154734050-154734333 | Common:10; Rare:144 | ||||
| chr6:155313640-155314180 | Common:4; Rare:213 | ||||
| chr6:155314413-155314870 | Common:25; Rare:299 | ||||
| chr6:157323030-157323300 | Rare:73 | ||||
| chr6:157323477-157323642 | Common:4; Rare:100 |