Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28645106-28645304 | Common:1; Rare:73 | ||||
chr17:28661888-28662298 | Common:1; Rare:144 | ||||
chr17:28812400-28812695 | Common:1; Rare:78 | ||||
chr17:28854984-28855032 | Rare:15 | ||||
chr17:32350060-32350194 | Rare:76 | ||||
chr17:34961453-34961575 | Common:1; Rare:59 | ||||
chr17:35242983-35243073 | Rare:31 | ||||
chr17:35809307-35809533 | Rare:90 | ||||
chr17:36486585-36486692 | Common:2; Rare:47 | ||||
chr17:36534799-36535034 | Common:3; Rare:103 | ||||
chr17:37406834-37406924 | Rare:28 | ||||
chr17:37489678-37489907 | Rare:91 | ||||
chr17:37609366-37609561 | Common:1; Rare:85 | ||||
chr17:37745057-37745369 | Rare:71; Clinvar (benign):2 | ||||
chr17:38752487-38752805 | Common:3; Rare:79 |