Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:59039057-59039199 | Common:1; Rare:45; Clinvar (benign):1 | ||||
chr5:59039312-59039707 | Common:3; Rare:88 | ||||
chr5:59275545-59275631 | Rare:14 | ||||
chr5:60488008-60488339 | Common:1; Rare:55 | ||||
chr5:60488342-60488384 | Rare:8 | ||||
chr5:60700102-60700237 | Common:1; Rare:52 | ||||
chr5:60945026-60945246 | Common:5; Rare:84; Clinvar:3; Clinvar (benign):5 | ||||
chr5:61162328-61162644 | Common:1; Rare:80 | ||||
chr5:62403821-62403958 | Common:1; Rare:56 | ||||
chr5:62412543-62412788 | Rare:79 | ||||
chr5:64165679-64165903 | Common:1; Rare:70 | ||||
chr5:64768409-64768457 | Common:2; Rare:15 | ||||
chr5:64768553-64769056 | Common:5; Rare:126 | ||||
chr5:65563124-65563421 | Common:3; Rare:118 | ||||
chr5:65624623-65624769 | Common:9; Rare:21 |