Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:75261583-75261931 | Common:4; Rare:108; Clinvar (benign):2 | ||||
chr17:75393824-75394077 | Common:1; Rare:60 | ||||
chr17:75667173-75667378 | Common:4; Rare:62 | ||||
chr17:75979126-75979283 | Rare:40; Clinvar:4 | ||||
chr17:76726462-76726872 | Common:5; Rare:153 | ||||
chr17:76737328-76737537 | Common:2; Rare:79 | ||||
chr17:78187045-78187364 | Common:3; Rare:100 | ||||
chr17:78840774-78841105 | Common:2; Rare:129 | ||||
chr17:80220317-80220429 | Rare:44; Clinvar:1 | ||||
chr17:81666552-81666758 | Common:1; Rare:88 | ||||
chr17:81683721-81684057 | Common:4; Rare:167 | ||||
chr17:81703297-81703493 | Common:2; Rare:55; Clinvar (benign):2 | ||||
chr17:81833257-81833339 | Rare:34 | ||||
chr17:81891374-81891768 | Common:3; Rare:151 | ||||
chr17:81937240-81937429 | Rare:70 |