Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:66593036-66593223 | Common:1; Rare:69 | ||||
chr11:66616356-66616672 | Common:1; Rare:101 | ||||
chr11:66638371-66638757 | Common:4; Rare:171 | ||||
chr11:66677796-66678092 | Common:1; Rare:106 | ||||
chr11:66744632-66744879 | Common:3; Rare:102 | ||||
chr11:67056727-67056882 | Common:1; Rare:44 | ||||
chr11:67353518-67353779 | Common:2; Rare:70 | ||||
chr11:67401774-67402075 | Common:3; Rare:113 | ||||
chr11:67428175-67428537 | Rare:110 | ||||
chr11:68030381-68030744 | Common:3; Rare:101; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271896-68272171 | Common:2; Rare:117 | ||||
chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
chr11:69048701-69049000 | Common:6; Rare:107 | ||||
chr11:69640972-69641259 | Common:1; Rare:59 | ||||
chr11:69641434-69641508 | Rare:14 |