Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:57961358-57961636 | Common:2; Rare:86 | ||||
chr6:63448267-63448528 | Common:1; Rare:39 | ||||
chr6:63458674-63459013 | Common:2; Rare:57 | ||||
chr6:63516194-63516479 | Common:4; Rare:57 | ||||
chr6:63553138-63553312 | Rare:31 | ||||
chr6:73517858-73518265 | Common:2; Rare:108 | ||||
chr6:79025564-79025830 | Rare:48; Clinvar (pathogenic):1 | ||||
chr6:81937451-81937732 | Common:1; Rare:64 | ||||
chr6:81938388-81938506 | Rare:20 | ||||
chr6:85678712-85678997 | Rare:102 | ||||
chr6:88662188-88662497 | Common:6; Rare:50 | ||||
chr6:88662569-88662745 | Rare:39 | ||||
chr6:88669496-88669791 | Common:2; Rare:51 | ||||
chr6:88670233-88670477 | Common:2; Rare:38 | ||||
chr6:89720876-89721155 | Common:2; Rare:45 |