| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:38033422-38033775 | Common:2; Rare:102 | ||||
| chr20:40689202-40689541 | Common:2; Rare:98 | ||||
| chr20:43590615-43590996 | Common:1; Rare:86 | ||||
| chr20:44210610-44211108 | Common:5; Rare:173 | ||||
| chr20:44909981-44910096 | Common:1; Rare:43 | ||||
| chr20:45406420-45406717 | Rare:75 | ||||
| chr20:45833571-45833851 | Common:4; Rare:60 | ||||
| chr20:45857339-45857634 | Common:3; Rare:79 | ||||
| chr20:45891186-45891419 | Common:1; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr20:45910895-45911193 | Common:4; Rare:91 | ||||
| chr20:46364366-46364575 | Common:1; Rare:76 | ||||
| chr20:49046183-49046347 | Common:3; Rare:47 | ||||
| chr20:49219258-49219441 | Common:1; Rare:89 | ||||
| chr20:49278036-49278248 | Rare:57 | ||||
| chr20:49568016-49568066 | Common:2; Rare:10 |