Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:25195596-25195769 | Common:2; Rare:59 | ||||
chr20:25623952-25624099 | Common:1; Rare:53 | ||||
chr20:25696800-25697051 | Common:3; Rare:73 | ||||
chr20:31547272-31547438 | Rare:45 | ||||
chr20:31722783-31722821 | Rare:8 | ||||
chr20:31739101-31739357 | Common:1; Rare:64 | ||||
chr20:32207665-32207944 | Common:3; Rare:105 | ||||
chr20:33401493-33401582 | Rare:24 | ||||
chr20:35284552-35284870 | Common:2; Rare:85 | ||||
chr20:35699305-35699456 | Rare:50; Clinvar (benign):3 | ||||
chr20:36236408-36236491 | Common:1; Rare:17 | ||||
chr20:36461144-36461486 | Common:1; Rare:100 | ||||
chr20:36746065-36746291 | Common:2; Rare:82 | ||||
chr20:37289492-37289669 | Common:1; Rare:49 | ||||
chr20:37527827-37528191 | Common:5; Rare:129 |