| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:18137754-18138039 | Common:2; Rare:101 | ||||
| chr20:18288458-18288588 | Rare:34 | ||||
| chr20:18467288-18467448 | Common:1; Rare:30 | ||||
| chr20:18497159-18497308 | Common:1; Rare:56 | ||||
| chr20:18507441-18507590 | Rare:37 | ||||
| chr20:18507691-18507961 | Common:2; Rare:82; Clinvar:5; Clinvar (benign):2 | ||||
| chr20:18567295-18567510 | Common:3; Rare:78 | ||||
| chr20:21125803-21126171 | Common:3; Rare:134; Clinvar (pathogenic):1 | ||||
| chr20:21303261-21303462 | Rare:70 | ||||
| chr20:21303515-21303826 | Common:1; Rare:85 | ||||
| chr20:24992702-24992827 | Common:3; Rare:56 | ||||
| chr20:25195598-25195780 | Common:2; Rare:62 | ||||
| chr20:25407506-25407778 | Common:3; Rare:93; Clinvar (pathogenic):1 | ||||
| chr20:25623952-25624056 | Common:1; Rare:38 | ||||
| chr20:25624414-25624642 | Common:2; Rare:56 |