| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:149749521-149749796 | Rare:122 | ||||
| chr6:150866358-150866512 | Rare:61 | ||||
| chr6:151325475-151325699 | Common:2; Rare:55 | ||||
| chr6:151391509-151391823 | Common:3; Rare:84 | ||||
| chr6:151452047-151452548 | Common:4; Rare:179 | ||||
| chr6:152168275-152168460 | Rare:39 | ||||
| chr6:153002467-153002838 | Common:5; Rare:149 | ||||
| chr6:154510579-154510799 | Common:2; Rare:68 | ||||
| chr6:157323501-157323642 | Common:2; Rare:42 | ||||
| chr6:158168203-158168393 | Common:2; Rare:67 | ||||
| chr6:158231888-158232266 | Common:1; Rare:117 | ||||
| chr6:158644686-158644945 | Common:3; Rare:103 | ||||
| chr6:158818084-158818350 | Common:4; Rare:105 | ||||
| chr6:158819322-158819565 | Common:2; Rare:93 | ||||
| chr6:158999761-158999886 | Common:1; Rare:47; Clinvar:1; Clinvar (benign):1 |