| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:52191482-52191663 | Rare:62 | ||||
| chr20:52191665-52191959 | Common:1; Rare:70 | ||||
| chr20:52192248-52192490 | Rare:38 | ||||
| chr20:53593771-53593914 | Common:1; Rare:54 | ||||
| chr20:53594157-53594274 | Rare:40 | ||||
| chr20:53609543-53609555 | Rare:2 | ||||
| chr20:54208060-54208212 | Rare:51 | ||||
| chr20:56391995-56392729 | Common:8; Rare:197 | ||||
| chr20:56468328-56468761 | Rare:133 | ||||
| chr20:57351116-57351482 | Common:2; Rare:110 | ||||
| chr20:57391115-57391415 | Common:7; Rare:117 | ||||
| chr20:57391878-57392090 | Common:5; Rare:50 | ||||
| chr20:58309372-58309824 | Common:3; Rare:193 | ||||
| chr20:58309959-58310185 | Common:1; Rare:60 | ||||
| chr20:58388960-58389336 | Common:4; Rare:182; Clinvar:5; Clinvar (benign):2 |