Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:44127354-44127675 | Common:4; Rare:94 | ||||
chr6:46652707-46653008 | Rare:76 | ||||
chr6:47477683-47477981 | Common:2; Rare:78; Clinvar:3; Clinvar (benign):3 | ||||
chr6:49463180-49463398 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr6:52995255-52995825 | Common:4; Rare:230 | ||||
chr6:53065379-53065608 | Common:1; Rare:69 | ||||
chr6:53348898-53349128 | Common:2; Rare:92 | ||||
chr6:54846439-54846820 | Common:2; Rare:93 | ||||
chr6:63572382-63572556 | Rare:66 | ||||
chr6:69796862-69797182 | Common:1; Rare:96; Clinvar:6; Clinvar (benign):3 | ||||
chr6:70413222-70413624 | Common:2; Rare:116 | ||||
chr6:73394530-73394898 | Common:6; Rare:105 | ||||
chr6:73461686-73461818 | Common:1; Rare:43; Clinvar (benign):1 | ||||
chr6:73653919-73654151 | Common:2; Rare:60; Clinvar:3 | ||||
chr6:73696017-73696236 | Common:1; Rare:54 |