| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:5001443-5001669 | Common:1; Rare:62 | ||||
| chr20:5112742-5113161 | Common:2; Rare:133 | ||||
| chr20:5119576-5120174 | Common:1; Rare:185 | ||||
| chr20:5950403-5950695 | Common:8; Rare:90 | ||||
| chr20:10434131-10434298 | Common:2; Rare:63; Clinvar (benign):1 | ||||
| chr20:13784865-13785080 | Common:2; Rare:94; Clinvar (benign):3 | ||||
| chr20:13785343-13785397 | Rare:12 | ||||
| chr20:13995277-13995551 | Rare:71 | ||||
| chr20:16573288-16573540 | Common:1; Rare:72 | ||||
| chr20:17682029-17682587 | Common:6; Rare:169 | ||||
| chr20:17968415-17968614 | Common:4; Rare:87 | ||||
| chr20:17968770-17969141 | Common:4; Rare:129 | ||||
| chr20:18467162-18467439 | Common:1; Rare:54 | ||||
| chr20:18507464-18507631 | Rare:43; Clinvar:1 | ||||
| chr20:18507771-18507957 | Common:1; Rare:53; Clinvar:5; Clinvar (benign):1 |