| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151391511-151391793 | Common:3; Rare:72 | ||||
| chr6:151452007-151452552 | Common:5; Rare:190; Clinvar (benign):3 | ||||
| chr6:152302056-152302206 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983005-152983281 | Common:2; Rare:83 | ||||
| chr6:152983508-152983760 | Common:4; Rare:96 | ||||
| chr6:153002634-153002838 | Common:3; Rare:77 | ||||
| chr6:153131200-153131491 | Rare:124 | ||||
| chr6:154510553-154510776 | Common:2; Rare:68 | ||||
| chr6:154733223-154733434 | Rare:82 | ||||
| chr6:155314426-155314630 | Common:4; Rare:76 | ||||
| chr6:157323473-157323642 | Common:2; Rare:60 | ||||
| chr6:158168177-158168409 | Common:3; Rare:86; Clinvar:1 | ||||
| chr6:158644704-158644894 | Common:2; Rare:81 | ||||
| chr6:158649872-158650059 | Rare:37 | ||||
| chr6:158818161-158818358 | Common:4; Rare:73 |