Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:53348892-53349099 | Common:2; Rare:86 | ||||
chr6:56542894-56543076 | Common:1; Rare:28 | ||||
chr6:57046481-57046747 | Rare:92 | ||||
chr6:57317547-57317667 | Rare:38 | ||||
chr6:63572274-63572562 | Rare:110 | ||||
chr6:69796877-69797151 | Common:1; Rare:80; Clinvar:4; Clinvar (benign):2 | ||||
chr6:73521186-73521411 | Common:1; Rare:43 | ||||
chr6:73696110-73696220 | Rare:23 | ||||
chr6:75284722-75285033 | Common:1; Rare:89 | ||||
chr6:75748954-75749258 | Common:6; Rare:100; Clinvar:2 | ||||
chr6:78867465-78867607 | Rare:64 | ||||
chr6:79078187-79078588 | Common:1; Rare:170 | ||||
chr6:79537373-79537611 | Common:1; Rare:66; Clinvar:3 | ||||
chr6:79631193-79631303 | Common:1; Rare:25 | ||||
chr6:80004483-80004710 | Common:4; Rare:55 |