| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:143060768-143060919 | Common:6; Rare:56 | ||||
| chr6:143450654-143450934 | Common:1; Rare:104; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:144285172-144285510 | Common:3; Rare:89 | ||||
| chr6:145814666-145814921 | Common:1; Rare:114 | ||||
| chr6:149545994-149546149 | Rare:65 | ||||
| chr6:149749617-149749796 | Rare:98 | ||||
| chr6:151452043-151452538 | Common:4; Rare:175 | ||||
| chr6:152302102-152302302 | Common:1; Rare:60 | ||||
| chr6:155314456-155314613 | Common:2; Rare:48 | ||||
| chr6:157323486-157323597 | Common:2; Rare:46 | ||||
| chr6:158168219-158168388 | Common:2; Rare:61 | ||||
| chr6:158644710-158644865 | Common:2; Rare:65 | ||||
| chr6:158649872-158650053 | Rare:36 | ||||
| chr6:158818207-158818537 | Common:7; Rare:113 | ||||
| chr6:158819335-158819565 | Common:2; Rare:84 |