| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39380211-39380493 | Common:1; Rare:131 | ||||
| chr21:39387608-39387808 | Common:2; Rare:76 | ||||
| chr21:39445765-39445901 | Common:2; Rare:45 | ||||
| chr21:42893066-42893336 | Common:4; Rare:88 | ||||
| chr21:44873605-44874040 | Common:8; Rare:176 | ||||
| chr21:45287843-45288093 | Common:6; Rare:98 | ||||
| chr21:45981519-45981838 | Common:23; Rare:77; Clinvar (benign):2 | ||||
| chr21:45986960-45987175 | Common:2; Rare:80; Clinvar:17; Clinvar (benign):8 | ||||
| chr21:46286252-46286396 | Common:4; Rare:53 | ||||
| chr21:46286580-46286642 | Common:1; Rare:20 | ||||
| chr21:46323823-46324165 | Common:2; Rare:114; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17628706-17628860 | Common:1; Rare:49 | ||||
| chr22:17638660-17638811 | Rare:51 | ||||
| chr22:18077829-18078006 | Common:3; Rare:60; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:19432284-19432606 | Common:4; Rare:138 |