| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:33542805-33543169 | Common:3; Rare:122 | ||||
| chr21:33641686-33642002 | Common:1; Rare:87 | ||||
| chr21:33642195-33642541 | Common:1; Rare:136 | ||||
| chr21:33931040-33931235 | Common:2; Rare:47 | ||||
| chr21:34073143-34073211 | Common:1; Rare:13 | ||||
| chr21:36060304-36060613 | Common:5; Rare:84 | ||||
| chr21:36319983-36320261 | Common:4; Rare:135 | ||||
| chr21:36966357-36966525 | Common:1; Rare:48 | ||||
| chr21:36990184-36990279 | Common:4; Rare:34; Clinvar (benign):4 | ||||
| chr21:37072511-37072741 | Common:5; Rare:118; Clinvar (pathogenic):1 | ||||
| chr21:37072783-37073390 | Common:8; Rare:217 | ||||
| chr21:37267304-37267706 | Common:4; Rare:142 | ||||
| chr21:37268074-37268251 | Common:3; Rare:44 | ||||
| chr21:39183858-39183964 | Common:1; Rare:47 | ||||
| chr21:39313487-39313930 | Common:9; Rare:245 |