| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:31659551-31659835 | Common:2; Rare:121; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):7 | ||||
| chr21:31732116-31732300 | Common:3; Rare:79 | ||||
| chr21:32278999-32279174 | Common:2; Rare:83 | ||||
| chr21:32392957-32393179 | Common:2; Rare:94 | ||||
| chr21:32612305-32612872 | Common:1; Rare:136 | ||||
| chr21:32727897-32728139 | Rare:118; Clinvar:2 | ||||
| chr21:33266299-33266434 | Rare:45; Clinvar:3 | ||||
| chr21:33324813-33325024 | Common:4; Rare:78 | ||||
| chr21:33403288-33403583 | Common:1; Rare:74; Clinvar:1 | ||||
| chr21:33479904-33480204 | Common:1; Rare:91 | ||||
| chr21:33491700-33491869 | Rare:40 | ||||
| chr21:33542073-33542263 | Rare:74 | ||||
| chr21:33542803-33543169 | Common:3; Rare:122 | ||||
| chr21:34526935-34527232 | Common:1; Rare:42 | ||||
| chr21:36060508-36060607 | Common:1; Rare:30 |