Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48610563-48610646 | Rare:26 | ||||
chr17:48944790-48944861 | Rare:16 | ||||
chr17:50373166-50373246 | Common:3; Rare:31 | ||||
chr17:54968619-54968749 | Common:3; Rare:67 | ||||
chr17:57850012-57850274 | Common:1; Rare:81 | ||||
chr17:57988246-57988512 | Common:5; Rare:73 | ||||
chr17:58352140-58352372 | Common:4; Rare:109 | ||||
chr17:58692361-58692663 | Common:2; Rare:125; Clinvar:9; Clinvar (benign):19 | ||||
chr17:59106727-59106999 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155143-59155523 | Common:2; Rare:87 | ||||
chr17:59565514-59565637 | Rare:45 | ||||
chr17:59619574-59619935 | Common:3; Rare:128 | ||||
chr17:59707401-59707730 | Common:3; Rare:89; Clinvar (benign):3 | ||||
chr17:59837722-59837943 | Rare:31 | ||||
chr17:59892900-59893137 | Rare:66 |