Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:2593861-2593957 | Common:1; Rare:33; Clinvar:2; Clinvar (benign):3 | ||||
chr17:3636241-3636501 | Common:4; Rare:73; Clinvar (benign):1 | ||||
chr17:3668552-3668829 | Common:2; Rare:108 | ||||
chr17:4143028-4143225 | Rare:64 | ||||
chr17:4143647-4143757 | Common:1; Rare:64 | ||||
chr17:4704108-4704245 | Rare:75 | ||||
chr17:4807004-4807210 | Common:4; Rare:64 | ||||
chr17:4939914-4940348 | Common:2; Rare:128 | ||||
chr17:4948954-4949011 | Common:1; Rare:15 | ||||
chr17:4967800-4968114 | Common:1; Rare:99 | ||||
chr17:5191838-5192073 | Common:1; Rare:79 | ||||
chr17:5419646-5419869 | Common:3; Rare:67 | ||||
chr17:5486154-5486400 | Common:4; Rare:106 | ||||
chr17:6640646-6641097 | Common:7; Rare:141 | ||||
chr17:6651574-6651734 | Common:1; Rare:51 |