| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:37366664-37366882 | Common:1; Rare:74 | ||||
| chr21:38498369-38498759 | Common:2; Rare:58 | ||||
| chr21:38660638-38660859 | Common:1; Rare:53 | ||||
| chr21:38804957-38805186 | Common:2; Rare:60 | ||||
| chr21:38805524-38806119 | Common:3; Rare:174 | ||||
| chr21:38809340-38809604 | Rare:34 | ||||
| chr21:39387635-39387793 | Common:2; Rare:67 | ||||
| chr21:39445751-39445932 | Common:3; Rare:58 | ||||
| chr21:41361907-41362048 | Common:1; Rare:18 | ||||
| chr21:41420422-41420650 | Common:3; Rare:51 | ||||
| chr21:41426068-41426263 | Common:3; Rare:45 | ||||
| chr21:41766983-41767175 | Common:5; Rare:86; Clinvar:1; Clinvar (benign):2 | ||||
| chr21:41879320-41879606 | Common:5; Rare:88 | ||||
| chr21:42879032-42879134 | Common:1; Rare:31 | ||||
| chr21:42879511-42879667 | Common:3; Rare:57 |