| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:20017242-20017372 | Rare:47 | ||||
| chr20:21125836-21126133 | Common:3; Rare:109 | ||||
| chr20:21303229-21303462 | Rare:77 | ||||
| chr20:23049623-23049939 | Common:3; Rare:102; Clinvar (pathogenic):1 | ||||
| chr20:23086310-23086478 | Rare:30 | ||||
| chr20:23350510-23350838 | Common:3; Rare:94 | ||||
| chr20:23361853-23362173 | Common:3; Rare:101 | ||||
| chr20:24992698-24992885 | Common:6; Rare:92 | ||||
| chr20:25057821-25058176 | Common:6; Rare:101 | ||||
| chr20:25195629-25195842 | Common:4; Rare:71 | ||||
| chr20:25247967-25248104 | Common:1; Rare:52 | ||||
| chr20:25623952-25624140 | Common:1; Rare:63 | ||||
| chr20:25624407-25624621 | Common:2; Rare:53 | ||||
| chr20:25696780-25696912 | Common:1; Rare:39 | ||||
| chr20:31547294-31547432 | Rare:30 |