| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149941755-149942152 | Common:8; Rare:104 | ||||
| chr6:149963829-149964011 | Common:1; Rare:56 | ||||
| chr6:150865547-150865721 | Rare:42 | ||||
| chr6:150866302-150866510 | Rare:85 | ||||
| chr6:151325169-151325311 | Rare:24 | ||||
| chr6:151325448-151326203 | Common:2; Rare:169 | ||||
| chr6:151391511-151391895 | Common:3; Rare:109 | ||||
| chr6:151452018-151452584 | Common:5; Rare:203; Clinvar (benign):3 | ||||
| chr6:152982860-152982931 | Common:1; Rare:23 | ||||
| chr6:152983009-152983351 | Common:2; Rare:105 | ||||
| chr6:152983516-152983743 | Common:3; Rare:87 | ||||
| chr6:153002666-153002863 | Common:4; Rare:66 | ||||
| chr6:153131219-153131460 | Rare:104 | ||||
| chr6:154510160-154510259 | Common:1; Rare:20 | ||||
| chr6:154510264-154510354 | Rare:21 |