| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33642170-33642591 | Common:2; Rare:155 | ||||
| chr21:34073070-34073241 | Common:2; Rare:50 | ||||
| chr21:34520887-34521126 | Rare:39 | ||||
| chr21:34526661-34527118 | Common:2; Rare:99 | ||||
| chr21:34886924-34887274 | Common:4; Rare:109; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr21:34887894-34888205 | Common:1; Rare:58 | ||||
| chr21:34888390-34888435 | Rare:13 | ||||
| chr21:34888677-34888840 | Rare:49 | ||||
| chr21:34889727-34889839 | Rare:38 | ||||
| chr21:36043555-36043837 | Rare:57 | ||||
| chr21:36070188-36070413 | Common:1; Rare:108 | ||||
| chr21:36134944-36135128 | Rare:47 | ||||
| chr21:36319929-36320270 | Common:4; Rare:161 | ||||
| chr21:36385346-36385440 | Rare:42 | ||||
| chr21:36698985-36699146 | Common:2; Rare:48 |