| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36319988-36320258 | Common:4; Rare:131 | ||||
| chr21:37072520-37072682 | Common:4; Rare:84 | ||||
| chr21:37072998-37073375 | Common:5; Rare:147 | ||||
| chr21:37267290-37267692 | Common:4; Rare:145 | ||||
| chr21:39380188-39380504 | Common:1; Rare:143 | ||||
| chr21:39445742-39445919 | Common:3; Rare:59 | ||||
| chr21:41426075-41426247 | Common:3; Rare:39 | ||||
| chr21:41508151-41508347 | Common:1; Rare:37 | ||||
| chr21:42496205-42496572 | Common:2; Rare:89 | ||||
| chr21:42653461-42653789 | Common:5; Rare:49 | ||||
| chr21:42893042-42893336 | Common:4; Rare:95 | ||||
| chr21:43659468-43659610 | Common:1; Rare:47 | ||||
| chr21:43776236-43776492 | Common:5; Rare:95; Clinvar:4; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr21:43789262-43789562 | Common:1; Rare:87 | ||||
| chr21:44801774-44801857 | Rare:37 |