| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:53077650-53077937 | Common:1; Rare:48 | ||||
| chr20:53078896-53079000 | Common:2; Rare:22 | ||||
| chr20:53079184-53079402 | Common:1; Rare:36 | ||||
| chr20:56787653-56787862 | Common:2; Rare:33 | ||||
| chr20:57126532-57126638 | Common:2; Rare:24 | ||||
| chr20:62307657-62308182 | Common:5; Rare:192 | ||||
| chr20:62308369-62308699 | Common:2; Rare:111 | ||||
| chr20:62776854-62777115 | Common:5; Rare:45 | ||||
| chr20:63365269-63365486 | Common:2; Rare:61 | ||||
| chr20:63864266-63864371 | Rare:23 | ||||
| chr20:63865892-63865947 | Common:1; Rare:14 | ||||
| chr21:6098444-6098762 | Rare:9 | ||||
| chr21:16194248-16194612 | Common:2; Rare:101 | ||||
| chr21:31667031-31667372 | Rare:85; Clinvar:1; Clinvar (pathogenic):9 | ||||
| chr21:31668405-31668509 | Rare:34; Clinvar (pathogenic):1 |