| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33642170-33642633 | Common:4; Rare:318 | ||||
| chr21:33915597-33916251 | Common:4; Rare:303 | ||||
| chr21:34073193-34073724 | Common:1; Rare:311 | ||||
| chr21:34887670-34888400 | Common:2; Rare:145 | ||||
| chr21:34888636-34888912 | Common:1; Rare:184 | ||||
| chr21:34889705-34889841 | Common:1; Rare:85 | ||||
| chr21:36060290-36060680 | Common:12; Rare:199 | ||||
| chr21:36069752-36070055 | Common:13; Rare:133 | ||||
| chr21:36156301-36156969 | Common:20; Rare:546 | ||||
| chr21:36319933-36320253 | Common:6; Rare:212 | ||||
| chr21:36385275-36385441 | Rare:63 | ||||
| chr21:36698896-36699228 | Common:5; Rare:163 | ||||
| chr21:36966273-36966970 | Common:14; Rare:301 | ||||
| chr21:36989750-36990090 | Common:11; Rare:169 | ||||
| chr21:37072480-37072920 | Common:13; Rare:297; Clinvar (pathogenic):1 |