Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35664886-35665015 | Common:1; Rare:32 | ||||
chr20:35699181-35699274 | Rare:13 | ||||
chr20:35699292-35699466 | Rare:61; Clinvar (benign):3 | ||||
chr20:35742175-35742651 | Common:5; Rare:153 | ||||
chr20:36461135-36461478 | Common:1; Rare:97 | ||||
chr20:36746065-36746291 | Common:2; Rare:82 | ||||
chr20:36773716-36773958 | Common:3; Rare:82 | ||||
chr20:37095919-37096269 | Common:1; Rare:118 | ||||
chr20:37289538-37289669 | Common:1; Rare:36 | ||||
chr20:37527827-37528159 | Common:3; Rare:115 | ||||
chr20:38033416-38033563 | Common:1; Rare:47 | ||||
chr20:38962132-38962383 | Common:1; Rare:103 | ||||
chr20:41028564-41028878 | Rare:116 | ||||
chr20:43590895-43590983 | Rare:21 | ||||
chr20:44187140-44187252 | Common:1; Rare:26 |