| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63707300-63707416 | Rare:40 | ||||
| chr20:63707881-63708118 | Rare:69 | ||||
| chr20:63865065-63865351 | Common:2; Rare:108 | ||||
| chr20:63969913-63970095 | Common:3; Rare:57 | ||||
| chr20:63979438-63979638 | Rare:50 | ||||
| chr20:64079924-64080111 | Common:2; Rare:79 | ||||
| chr20:64255637-64255796 | Common:3; Rare:79 | ||||
| chr21:14383110-14383479 | Common:2; Rare:105 | ||||
| chr21:25607473-25607545 | Rare:41 | ||||
| chr21:25734864-25735497 | Common:5; Rare:219 | ||||
| chr21:25735584-25735796 | Common:1; Rare:52 | ||||
| chr21:26170568-26170842 | Common:3; Rare:94; Clinvar:5; Clinvar (benign):2 | ||||
| chr21:26845327-26845664 | Common:2; Rare:96 | ||||
| chr21:29073561-29073870 | Common:2; Rare:96 | ||||
| chr21:29298631-29298965 | Common:3; Rare:135 |