Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:34303290-34303357 | Common:1; Rare:48; Clinvar:2; Clinvar (benign):1 | ||||
chr20:34677086-34677288 | Rare:53 | ||||
chr20:35147293-35147405 | Rare:36 | ||||
chr20:35455051-35455210 | Common:1; Rare:56 | ||||
chr20:35664880-35665004 | Common:1; Rare:33 | ||||
chr20:35699336-35699456 | Rare:35 | ||||
chr20:35742182-35742651 | Common:5; Rare:152 | ||||
chr20:36236374-36236483 | Common:2; Rare:27 | ||||
chr20:36605537-36605796 | Common:2; Rare:92 | ||||
chr20:36746059-36746311 | Common:2; Rare:88 | ||||
chr20:37178865-37179173 | Rare:87 | ||||
chr20:37527836-37528207 | Common:5; Rare:134 | ||||
chr20:38033397-38033552 | Common:1; Rare:48 | ||||
chr20:38165262-38165396 | Rare:39 | ||||
chr20:41028462-41028851 | Rare:129 |