| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:45541692-45542092 | Common:5; Rare:200 | ||||
| chr21:45542353-45542757 | Rare:242 | ||||
| chr21:45747710-45748270 | Common:3; Rare:239 | ||||
| chr21:45748715-45749210 | Common:7; Rare:110 | ||||
| chr21:45981468-45981790 | Common:46; Rare:122; Clinvar (benign):3 | ||||
| chr21:46097900-46098180 | Common:1; Rare:130; Clinvar (benign):2 | ||||
| chr21:46184404-46184761 | Common:4; Rare:32 | ||||
| chr21:46228484-46228847 | Common:3; Rare:263 | ||||
| chr21:46228863-46229329 | Common:15; Rare:220 | ||||
| chr21:46285764-46285952 | Common:2; Rare:74 | ||||
| chr21:46286006-46286760 | Common:18; Rare:535 | ||||
| chr21:46323639-46324268 | Common:10; Rare:617; Clinvar:12; Clinvar (benign):6 | ||||
| chr21:46324363-46325012 | Common:25; Rare:535 | ||||
| chr21:46325271-46325488 | Common:2; Rare:85 | ||||
| chr21:46458422-46459217 | Common:16; Rare:614 |