| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:48921399-48922417 | Common:12; Rare:653; Clinvar:13; Clinvar (benign):11 | ||||
| chr20:49046102-49046415 | Common:9; Rare:246 | ||||
| chr20:49046574-49046986 | Common:10; Rare:277 | ||||
| chr20:49187188-49188003 | Common:7; Rare:282 | ||||
| chr20:49188109-49188715 | Common:12; Rare:551 | ||||
| chr20:49219153-49219566 | Common:4; Rare:447 | ||||
| chr20:49277959-49278326 | Common:1; Rare:219 | ||||
| chr20:49278356-49278740 | Common:31; Rare:344 | ||||
| chr20:49484159-49484559 | Common:7; Rare:218 | ||||
| chr20:49712790-49713520 | Common:9; Rare:295 | ||||
| chr20:49713792-49714091 | Common:2; Rare:158 | ||||
| chr20:49812542-49812983 | Common:13; Rare:257 | ||||
| chr20:49812970-49813190 | Common:10; Rare:125 | ||||
| chr20:49813208-49813359 | Common:7; Rare:45 | ||||
| chr20:49915257-49915938 | Common:14; Rare:402 |