Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:35699336-35699460 | Rare:38 | ||||
chr20:36236374-36236491 | Common:2; Rare:29 | ||||
chr20:36746062-36746212 | Common:2; Rare:65 | ||||
chr20:36951679-36951913 | Common:1; Rare:56; Clinvar (benign):3 | ||||
chr20:37178972-37179156 | Rare:55 | ||||
chr20:37289545-37289682 | Common:1; Rare:44 | ||||
chr20:37527834-37528196 | Common:5; Rare:129 | ||||
chr20:38033407-38033767 | Common:2; Rare:105 | ||||
chr20:43458259-43458401 | Common:2; Rare:60 | ||||
chr20:44210710-44211037 | Common:4; Rare:124 | ||||
chr20:44966391-44966550 | Rare:59 | ||||
chr20:45791917-45792002 | Common:1; Rare:32 | ||||
chr20:45812301-45812750 | Common:4; Rare:130 | ||||
chr20:45857343-45857616 | Common:3; Rare:70 | ||||
chr20:45881018-45881232 | Common:2; Rare:49 |