| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:151325410-151325707 | Common:2; Rare:68 | ||||
| chr6:151452019-151452548 | Common:5; Rare:189; Clinvar (benign):3 | ||||
| chr6:152983021-152983337 | Common:2; Rare:97 | ||||
| chr6:153002634-153002861 | Common:4; Rare:85 | ||||
| chr6:157323497-157323642 | Common:2; Rare:45 | ||||
| chr6:158168187-158168388 | Common:3; Rare:71 | ||||
| chr6:158644704-158644930 | Common:2; Rare:89 | ||||
| chr6:158819333-158819535 | Common:2; Rare:75 | ||||
| chr6:159727030-159727176 | Rare:50 | ||||
| chr6:159761876-159762067 | Common:3; Rare:103 | ||||
| chr6:159789545-159789970 | Common:4; Rare:143 | ||||
| chr6:162727766-162728019 | Common:2; Rare:69; Clinvar:1 | ||||
| chr6:166342477-166342663 | Common:5; Rare:79 | ||||
| chr6:166999074-166999404 | Common:1; Rare:112 | ||||
| chr6:169702021-169702138 | Common:1; Rare:46 |