| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:20367929-20368106 | Common:1; Rare:59 | ||||
| chr20:21125791-21126123 | Common:3; Rare:117 | ||||
| chr20:21302990-21303410 | Rare:135 | ||||
| chr20:21303703-21303851 | Rare:44 | ||||
| chr20:23350481-23350898 | Common:4; Rare:128 | ||||
| chr20:23361863-23362240 | Common:3; Rare:126 | ||||
| chr20:23421394-23421636 | Common:4; Rare:104 | ||||
| chr20:23452864-23453186 | Common:1; Rare:57 | ||||
| chr20:24992601-24992873 | Common:8; Rare:128 | ||||
| chr20:25195609-25195784 | Common:2; Rare:61 | ||||
| chr20:25247967-25248108 | Common:1; Rare:54 | ||||
| chr20:25390770-25391054 | Common:2; Rare:105; Clinvar:3; Clinvar (benign):2 | ||||
| chr20:25407556-25407882 | Common:1; Rare:128; Clinvar (pathogenic):1 | ||||
| chr20:25585474-25585760 | Common:3; Rare:81 | ||||
| chr20:25623923-25624053 | Common:1; Rare:62 |