| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:136289756-136290020 | Common:1; Rare:113 | ||||
| chr6:137219111-137219229 | Common:1; Rare:40; Clinvar:1 | ||||
| chr6:138404167-138404555 | Common:7; Rare:110 | ||||
| chr6:142147135-142147284 | Rare:52 | ||||
| chr6:143060731-143060919 | Common:7; Rare:65 | ||||
| chr6:143450684-143450929 | Common:1; Rare:87; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:145814731-145814921 | Common:1; Rare:91 | ||||
| chr6:149546001-149546166 | Common:1; Rare:69 | ||||
| chr6:149749564-149749788 | Rare:108 | ||||
| chr6:151452047-151452531 | Common:4; Rare:170 | ||||
| chr6:152983027-152983303 | Common:2; Rare:90 | ||||
| chr6:153002652-153003033 | Common:5; Rare:125 | ||||
| chr6:157323495-157323621 | Common:2; Rare:43 | ||||
| chr6:158168230-158168388 | Common:2; Rare:56 | ||||
| chr6:158644703-158644927 | Common:2; Rare:90 |