Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:53061687-53061932 | Rare:57 | ||||
chr6:53065377-53065618 | Common:1; Rare:74 | ||||
chr6:53348848-53349222 | Common:2; Rare:155 | ||||
chr6:54846623-54846821 | Common:1; Rare:49 | ||||
chr6:57089894-57090206 | Rare:110 | ||||
chr6:57172530-57172766 | Common:1; Rare:77 | ||||
chr6:57317539-57317654 | Rare:32 | ||||
chr6:63572256-63572492 | Rare:91 | ||||
chr6:69796867-69797151 | Common:1; Rare:85; Clinvar:4; Clinvar (benign):2 | ||||
chr6:70667707-70667960 | Common:2; Rare:84 | ||||
chr6:73310152-73310274 | Common:1; Rare:32 | ||||
chr6:73520991-73521339 | Common:3; Rare:95 | ||||
chr6:73521537-73521655 | Rare:32 | ||||
chr6:73523816-73523867 | Rare:16 | ||||
chr6:73653883-73654183 | Common:3; Rare:82; Clinvar:3 |