| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:63409731-63409949 | Rare:31 | ||||
| chr20:63501932-63502308 | Common:5; Rare:82 | ||||
| chr20:63690652-63690852 | Rare:81; Clinvar (benign):3 | ||||
| chr20:63801220-63801509 | Common:2; Rare:75 | ||||
| chr20:63807964-63808111 | Common:2; Rare:34 | ||||
| chr20:63862470-63862499 | Rare:16 | ||||
| chr20:63864266-63864376 | Rare:23 | ||||
| chr20:63865892-63866187 | Common:1; Rare:73 | ||||
| chr21:6565160-6565424 | Rare:40 | ||||
| chr21:8849965-8849997 | Rare:2 | ||||
| chr21:9529636-9529940 | Rare:6 | ||||
| chr21:9757209-9757339 | Rare:1 | ||||
| chr21:9757474-9757605 | Rare:2 | ||||
| chr21:9839351-9839562 | Rare:9 | ||||
| chr21:10119394-10119571 | Common:1; Rare:19 |