Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2511820-2512021 | Common:2; Rare:61 | ||||
chr17:2593863-2593984 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
chr17:3668552-3668860 | Common:2; Rare:126 | ||||
chr17:3723764-3723925 | Common:1; Rare:89 | ||||
chr17:4143011-4143232 | Rare:72 | ||||
chr17:4143597-4143735 | Common:4; Rare:79 | ||||
chr17:4263943-4264060 | Rare:47 | ||||
chr17:4555312-4555548 | Common:3; Rare:108 | ||||
chr17:4704116-4704211 | Rare:56 | ||||
chr17:4731296-4731484 | Common:2; Rare:55 | ||||
chr17:4806987-4807216 | Common:4; Rare:70 | ||||
chr17:4939914-4940136 | Common:2; Rare:75 | ||||
chr17:5191838-5192077 | Common:1; Rare:79 | ||||
chr17:5419639-5419882 | Common:3; Rare:73 | ||||
chr17:5420091-5420207 | Rare:46 |