| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:62386953-62387382 | Common:3; Rare:157 | ||||
| chr20:62937877-62938193 | Common:2; Rare:116 | ||||
| chr20:62952570-62953091 | Common:7; Rare:158; Clinvar (pathogenic):1 | ||||
| chr20:63254400-63254650 | Rare:87 | ||||
| chr20:63574215-63574315 | Rare:26 | ||||
| chr20:63653384-63653633 | Common:2; Rare:29 | ||||
| chr20:63658233-63658364 | Common:4; Rare:43 | ||||
| chr20:63707865-63708118 | Rare:72 | ||||
| chr20:63865219-63865368 | Common:1; Rare:71 | ||||
| chr20:64079924-64080130 | Common:2; Rare:85 | ||||
| chr21:14383167-14383479 | Common:2; Rare:75 | ||||
| chr21:17819324-17819455 | Common:1; Rare:46 | ||||
| chr21:25607458-25607555 | Rare:54 | ||||
| chr21:25734851-25735485 | Common:5; Rare:218 | ||||
| chr21:25735521-25735721 | Rare:55 |