Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5486166-5486399 | Common:4; Rare:98 | ||||
chr17:6640646-6641100 | Common:7; Rare:144 | ||||
chr17:7012317-7012677 | Rare:126 | ||||
chr17:7251978-7252319 | Common:1; Rare:130 | ||||
chr17:7440500-7440794 | Rare:57 | ||||
chr17:7484247-7484370 | Common:1; Rare:50 | ||||
chr17:7583542-7583865 | Common:1; Rare:132; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr17:7584070-7584113 | Rare:8 | ||||
chr17:8162936-8163093 | Rare:51 | ||||
chr17:8176313-8176492 | Rare:57 | ||||
chr17:8435708-8436003 | Common:4; Rare:120 | ||||
chr17:10697503-10697654 | Common:3; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
chr17:14069440-14069569 | Common:2; Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
chr17:15699506-15699768 | Common:3; Rare:69 | ||||
chr17:15999593-16000032 | Common:3; Rare:187; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 |