| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47355605-47356008 | Rare:128 | ||||
| chr20:47356608-47357705 | Common:3; Rare:667 | ||||
| chr20:47501530-47502190 | Common:10; Rare:903 | ||||
| chr20:48827860-48828856 | Common:16; Rare:596 | ||||
| chr20:48921368-48921940 | Common:18; Rare:819; Clinvar:8; Clinvar (benign):8 | ||||
| chr20:48921958-48922158 | Rare:88; Clinvar:2 | ||||
| chr20:48922090-48922653 | Common:3; Rare:158 | ||||
| chr20:49046098-49046521 | Common:18; Rare:451 | ||||
| chr20:49046570-49046979 | Common:13; Rare:406 | ||||
| chr20:49188178-49188658 | Common:9; Rare:479 | ||||
| chr20:49219100-49219538 | Common:7; Rare:962 | ||||
| chr20:49277961-49279012 | Common:66; Rare:1307 | ||||
| chr20:49712708-49714146 | Common:24; Rare:1211 | ||||
| chr20:49812378-49813318 | Common:31; Rare:600 | ||||
| chr20:49915227-49915992 | Common:29; Rare:1012 |