Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32350012-32350224 | Rare:108 | ||||
chr17:34961423-34961569 | Common:1; Rare:74 | ||||
chr17:35242910-35243076 | Rare:54 | ||||
chr17:35433135-35433460 | Common:5; Rare:74 | ||||
chr17:35578551-35578684 | Common:1; Rare:32; Clinvar (benign):1 | ||||
chr17:35587184-35587530 | Rare:90 | ||||
chr17:35809272-35809524 | Rare:102 | ||||
chr17:36534795-36535039 | Common:3; Rare:106 | ||||
chr17:36544787-36544964 | Common:3; Rare:58 | ||||
chr17:37406812-37406924 | Rare:42 | ||||
chr17:37489651-37489919 | Rare:113 | ||||
chr17:37609362-37609561 | Common:1; Rare:87 | ||||
chr17:38752496-38752826 | Common:4; Rare:89 | ||||
chr17:38825292-38825405 | Common:1; Rare:33 | ||||
chr17:38853696-38853889 | Common:3; Rare:78 |