Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:44141769-44141936 | Common:1; Rare:33 | ||||
chr17:44186673-44187043 | Common:1; Rare:125 | ||||
chr17:44221241-44221353 | Rare:34 | ||||
chr17:44222111-44222321 | Rare:41 | ||||
chr17:44324774-44324993 | Common:2; Rare:80 | ||||
chr17:44503366-44503727 | Rare:137 | ||||
chr17:44899369-44899820 | Common:3; Rare:132; Clinvar:3; Clinvar (benign):1 | ||||
chr17:45060964-45061339 | Common:2; Rare:98 | ||||
chr17:45132333-45132631 | Common:2; Rare:88 | ||||
chr17:45148152-45148614 | Common:1; Rare:158 | ||||
chr17:46193378-46193603 | Common:3; Rare:59 | ||||
chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47189226-47189582 | Rare:87 | ||||
chr17:47323868-47324013 | Common:1; Rare:54 | ||||
chr17:47603831-47604030 | Rare:33 |