| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35284545-35284880 | Common:2; Rare:90 | ||||
| chr20:35699336-35699445 | Rare:29 | ||||
| chr20:38033423-38033521 | Rare:32 | ||||
| chr20:44210756-44211048 | Common:4; Rare:104 | ||||
| chr20:45791914-45791998 | Rare:34 | ||||
| chr20:45857371-45857614 | Common:3; Rare:56 | ||||
| chr20:49278045-49278239 | Rare:53 | ||||
| chr20:50958502-50958830 | Common:1; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr20:62937883-62938178 | Common:2; Rare:107 | ||||
| chr21:25734873-25735090 | Common:2; Rare:95 | ||||
| chr21:29073607-29073860 | Common:2; Rare:72 | ||||
| chr21:32392965-32393148 | Common:2; Rare:79 | ||||
| chr21:33542832-33543081 | Common:2; Rare:86 | ||||
| chr21:42893133-42893334 | Common:1; Rare:66 | ||||
| chr21:44299984-44300089 | Rare:41 |