| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:50958503-50958833 | Common:1; Rare:103; Clinvar (benign):2 | ||||
| chr20:56392182-56392468 | Common:1; Rare:83 | ||||
| chr20:58309426-58309763 | Common:2; Rare:137 | ||||
| chr20:58891216-58891421 | Common:4; Rare:80 | ||||
| chr20:62143288-62143778 | Common:7; Rare:204 | ||||
| chr20:62182953-62183044 | Rare:21 | ||||
| chr20:62238242-62238581 | Common:1; Rare:93 | ||||
| chr20:62386847-62387127 | Common:4; Rare:118 | ||||
| chr20:62952589-62952709 | Common:2; Rare:31 | ||||
| chr20:63520625-63520816 | Common:3; Rare:90 | ||||
| chr20:63658255-63658364 | Common:2; Rare:38 | ||||
| chr20:63707918-63708092 | Rare:48 | ||||
| chr20:64049637-64049874 | Common:1; Rare:57 | ||||
| chr21:25734870-25734954 | Common:2; Rare:36 | ||||
| chr21:26170677-26170867 | Common:3; Rare:68; Clinvar:4; Clinvar (benign):2 |