| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149718055-149718168 | Common:2; Rare:38 | ||||
| chr6:149746496-149746640 | Common:2; Rare:72 | ||||
| chr6:149749636-149749835 | Rare:102 | ||||
| chr6:151391491-151391857 | Common:3; Rare:104 | ||||
| chr6:151452032-151452548 | Common:4; Rare:182 | ||||
| chr6:152301888-152302223 | Common:1; Rare:114; Clinvar:9; Clinvar (benign):5 | ||||
| chr6:152302226-152302256 | Rare:13 | ||||
| chr6:152637334-152637581 | Rare:48 | ||||
| chr6:152983021-152983327 | Common:2; Rare:96 | ||||
| chr6:152983518-152983756 | Common:4; Rare:90 | ||||
| chr6:153002637-153002861 | Common:4; Rare:83 | ||||
| chr6:155013518-155013789 | Common:1; Rare:37 | ||||
| chr6:155216933-155216973 | Rare:6 | ||||
| chr6:157323503-157323658 | Common:3; Rare:44 | ||||
| chr6:158168170-158168393 | Common:3; Rare:85 |