| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:28992787-28993110 | Common:2; Rare:135 | ||||
| chr21:29019297-29019450 | Common:5; Rare:68 | ||||
| chr21:29024534-29024774 | Common:2; Rare:103 | ||||
| chr21:29024865-29025037 | Rare:33 | ||||
| chr21:29073505-29073872 | Common:2; Rare:113 | ||||
| chr21:29298643-29298963 | Common:3; Rare:130 | ||||
| chr21:29299159-29299205 | Rare:14 | ||||
| chr21:31559041-31559254 | Common:2; Rare:67 | ||||
| chr21:31559431-31559614 | Rare:57 | ||||
| chr21:31659491-31659840 | Common:2; Rare:156; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31731910-31732271 | Common:4; Rare:145 | ||||
| chr21:31872864-31873039 | Common:2; Rare:46 | ||||
| chr21:32278985-32279214 | Common:3; Rare:102 | ||||
| chr21:32392869-32393139 | Common:1; Rare:107 | ||||
| chr21:32412629-32412717 | Rare:17 |