| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44517319-44517662 | Common:2; Rare:122 | ||||
| chr21:44596216-44596391 | Common:8; Rare:30 | ||||
| chr21:44847033-44847182 | Common:1; Rare:43 | ||||
| chr21:44856315-44856436 | Common:1; Rare:42 | ||||
| chr21:44856467-44856624 | Rare:39 | ||||
| chr21:45004568-45004591 | Rare:5 | ||||
| chr21:45100849-45100951 | Common:1; Rare:22 | ||||
| chr21:45101072-45101286 | Common:1; Rare:62 | ||||
| chr21:45440482-45440741 | Common:1; Rare:55 | ||||
| chr21:45492243-45492562 | Common:1; Rare:89; Clinvar (benign):2 | ||||
| chr21:45590565-45590801 | Common:5; Rare:77 | ||||
| chr21:45705263-45705427 | Rare:23 | ||||
| chr21:45792987-45793027 | Rare:9 | ||||
| chr21:46022614-46022781 | Common:2; Rare:48 | ||||
| chr21:46033708-46033965 | Common:11; Rare:63 |