Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:84763442-84763653 | Rare:50 | ||||
chr6:84764572-84764707 | Rare:40 | ||||
chr6:85449939-85450152 | Common:1; Rare:63 | ||||
chr6:85593777-85594087 | Common:2; Rare:91 | ||||
chr6:85643817-85643931 | Common:2; Rare:36 | ||||
chr6:87155223-87155590 | Rare:96 | ||||
chr6:87589921-87590171 | Common:3; Rare:128; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr6:88963585-88963850 | Common:2; Rare:92 | ||||
chr6:89081049-89081335 | Rare:115 | ||||
chr6:89352619-89353005 | Common:2; Rare:89 | ||||
chr6:89638434-89638549 | Common:1; Rare:25 | ||||
chr6:89638713-89638829 | Common:3; Rare:43 | ||||
chr6:89819713-89819863 | Rare:53 | ||||
chr6:89829595-89829914 | Rare:77 | ||||
chr6:90587018-90587322 | Common:2; Rare:84 |