Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:83193222-83193389 | Common:3; Rare:58 | ||||
chr6:85449941-85450127 | Common:1; Rare:54 | ||||
chr6:85593804-85593952 | Rare:52 | ||||
chr6:85643296-85643659 | Common:2; Rare:120 | ||||
chr6:85643817-85643933 | Common:2; Rare:37 | ||||
chr6:87155268-87155588 | Rare:85 | ||||
chr6:87472900-87472996 | Common:1; Rare:38; Clinvar (benign):4 | ||||
chr6:87589953-87590169 | Common:3; Rare:98; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr6:88963585-88963830 | Common:2; Rare:83 | ||||
chr6:89080573-89080777 | Common:1; Rare:88 | ||||
chr6:89117950-89118085 | Common:1; Rare:56 | ||||
chr6:89411287-89411468 | Common:1; Rare:39 | ||||
chr6:89638721-89638824 | Common:3; Rare:36 | ||||
chr6:89819709-89820075 | Common:1; Rare:107 | ||||
chr6:89829594-89829914 | Rare:77 |