Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:57850006-57850274 | Common:1; Rare:86 | ||||
chr17:57988188-57988512 | Common:5; Rare:97 | ||||
chr17:58219226-58219372 | Common:1; Rare:59; Clinvar:2; Clinvar (benign):3 | ||||
chr17:58352140-58352495 | Common:6; Rare:135 | ||||
chr17:58692530-58692650 | Common:1; Rare:63; Clinvar:5; Clinvar (benign):16 | ||||
chr17:59106727-59107133 | Common:2; Rare:131; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155556-59155758 | Rare:53 | ||||
chr17:59220394-59220542 | Common:2; Rare:43 | ||||
chr17:59565490-59565637 | Rare:51 | ||||
chr17:59619569-59619983 | Common:3; Rare:148 | ||||
chr17:59707397-59707700 | Common:3; Rare:85; Clinvar (benign):3 | ||||
chr17:59892900-59893139 | Rare:66 | ||||
chr17:59964714-59965073 | Common:2; Rare:104 | ||||
chr17:60078917-60078976 | Common:4; Rare:30 | ||||
chr17:60305227-60305302 | Rare:16 |