Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:85449538-85449737 | Common:1; Rare:52 | ||||
chr6:85449822-85450179 | Common:1; Rare:100 | ||||
chr6:87155351-87155611 | Rare:77 | ||||
chr6:87589759-87590175 | Common:3; Rare:184; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
chr6:88963561-88963836 | Common:2; Rare:94 | ||||
chr6:89638424-89638524 | Common:1; Rare:20 | ||||
chr6:89638685-89638824 | Common:5; Rare:53 | ||||
chr6:89829605-89829937 | Rare:80 | ||||
chr6:95577414-95577598 | Common:5; Rare:54 | ||||
chr6:96521686-96521923 | Common:6; Rare:117 | ||||
chr6:96897672-96898084 | Common:5; Rare:149; Clinvar:4; Clinvar (benign):4 | ||||
chr6:99402790-99402893 | Common:2; Rare:25 | ||||
chr6:99425245-99425446 | Common:2; Rare:56 | ||||
chr6:100464876-100465105 | Common:2; Rare:63 | ||||
chr6:100881077-100881504 | Common:7; Rare:139 |