Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:32853664-32853888 | Common:1; Rare:89; Clinvar:2; Clinvar (benign):3 | ||||
chr6:32854010-32854224 | Common:2; Rare:54 | ||||
chr6:33200350-33200448 | Rare:26 | ||||
chr6:33200654-33200948 | Common:2; Rare:89 | ||||
chr6:33202668-33203012 | Rare:80 | ||||
chr6:33271830-33272125 | Common:1; Rare:119 | ||||
chr6:33288985-33289812 | Common:4; Rare:221 | ||||
chr6:33298924-33299044 | Rare:32 | ||||
chr6:33299417-33299510 | Common:1; Rare:22 | ||||
chr6:33320407-33320764 | Common:2; Rare:101; Clinvar (pathogenic):1 | ||||
chr6:33418030-33418454 | Common:2; Rare:101 | ||||
chr6:33454450-33454624 | Rare:41 | ||||
chr6:34426019-34426186 | Common:5; Rare:71; Clinvar:1; Clinvar (benign):8 | ||||
chr6:34696730-34696953 | Common:1; Rare:50 | ||||
chr6:34757293-34757551 | Common:1; Rare:73 |