Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:3846724-3846886 | Rare:48 | ||||
chr20:5119913-5120155 | Common:1; Rare:83 | ||||
chr20:5950414-5950695 | Common:8; Rare:86 | ||||
chr20:11890611-11890897 | Common:2; Rare:100 | ||||
chr20:13784884-13785053 | Common:2; Rare:70; Clinvar (benign):2 | ||||
chr20:13995286-13995526 | Rare:59 | ||||
chr20:16573288-16573543 | Common:1; Rare:74 | ||||
chr20:16729901-16730064 | Rare:49 | ||||
chr20:17968438-17968609 | Common:4; Rare:74 | ||||
chr20:17968788-17969090 | Common:2; Rare:114 | ||||
chr20:18467148-18467439 | Common:1; Rare:59 | ||||
chr20:21303181-21303385 | Rare:78 | ||||
chr20:23350501-23350851 | Common:4; Rare:105 | ||||
chr20:23361855-23362229 | Common:3; Rare:128 | ||||
chr20:24992702-24992827 | Common:3; Rare:56 |