Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:75243739-75243985 | Common:1; Rare:108 | ||||
chr6:75284701-75285083 | Common:1; Rare:117 | ||||
chr6:75749024-75749246 | Common:5; Rare:74; Clinvar:1 | ||||
chr6:78867471-78867563 | Rare:32 | ||||
chr6:79537346-79537650 | Common:2; Rare:92; Clinvar:4 | ||||
chr6:79630986-79631318 | Common:2; Rare:70 | ||||
chr6:81752659-81752851 | Rare:99 | ||||
chr6:82247704-82248018 | Common:1; Rare:100 | ||||
chr6:83193201-83193397 | Common:3; Rare:68 | ||||
chr6:85593804-85594027 | Rare:70 | ||||
chr6:85643808-85643933 | Common:2; Rare:38 | ||||
chr6:87155249-87155588 | Rare:88 | ||||
chr6:87589926-87590160 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr6:89080581-89080777 | Common:1; Rare:86 | ||||
chr6:89638721-89638824 | Common:3; Rare:36 |