| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:150599772-150599931 | Common:1; Rare:65 | ||||
| chr6:151325475-151325697 | Common:2; Rare:55 | ||||
| chr6:151391013-151391214 | Common:2; Rare:63 | ||||
| chr6:151391519-151391756 | Common:3; Rare:55 | ||||
| chr6:151452032-151452552 | Common:4; Rare:183 | ||||
| chr6:151493982-151494147 | Common:2; Rare:58 | ||||
| chr6:152302071-152302213 | Rare:46; Clinvar (benign):1 | ||||
| chr6:152983518-152983747 | Common:4; Rare:87 | ||||
| chr6:153002643-153002838 | Common:3; Rare:70 | ||||
| chr6:154510539-154510772 | Common:2; Rare:71 | ||||
| chr6:155314399-155314603 | Common:4; Rare:83 | ||||
| chr6:157323503-157323597 | Common:2; Rare:32 | ||||
| chr6:158168190-158168388 | Common:2; Rare:71 | ||||
| chr6:158644703-158644926 | Common:2; Rare:90 | ||||
| chr6:158649852-158650064 | Common:1; Rare:38 |