Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:31273618-31273650 | Rare:2 | ||||
chr17:31314019-31314229 | Rare:37 | ||||
chr17:31321608-31321630 | Rare:7 | ||||
chr17:32142372-32142620 | Common:8; Rare:110 | ||||
chr17:32350041-32350209 | Rare:91 | ||||
chr17:34255089-34255325 | Rare:62 | ||||
chr17:34961489-34961578 | Common:1; Rare:44 | ||||
chr17:34980378-34980604 | Common:4; Rare:65 | ||||
chr17:34981146-34981479 | Common:2; Rare:64 | ||||
chr17:35063662-35063836 | Rare:26 | ||||
chr17:35242910-35243087 | Rare:60 | ||||
chr17:35373582-35373841 | Common:5; Rare:51 | ||||
chr17:35578522-35578684 | Common:1; Rare:38; Clinvar (benign):1 | ||||
chr17:35731676-35731851 | Rare:54 | ||||
chr17:35809269-35809543 | Rare:116 |