| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36966349-36966509 | Common:2; Rare:45 | ||||
| chr21:36990191-36990279 | Common:4; Rare:32; Clinvar (benign):4 | ||||
| chr21:37072593-37072665 | Common:1; Rare:37 | ||||
| chr21:37073006-37073390 | Common:5; Rare:145 | ||||
| chr21:37267269-37267708 | Common:4; Rare:158 | ||||
| chr21:37267882-37267980 | Rare:33 | ||||
| chr21:37365820-37366103 | Common:1; Rare:91 | ||||
| chr21:38805021-38805203 | Common:2; Rare:46 | ||||
| chr21:38805554-38805933 | Common:1; Rare:101 | ||||
| chr21:39183381-39183604 | Common:6; Rare:91 | ||||
| chr21:39313443-39313746 | Common:9; Rare:161 | ||||
| chr21:39445765-39445919 | Common:2; Rare:51 | ||||
| chr21:41426033-41426279 | Common:3; Rare:58 | ||||
| chr21:41508035-41508349 | Common:2; Rare:68 | ||||
| chr21:41767037-41767183 | Common:3; Rare:69; Clinvar:1 |