Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:67239808-67240134 | Rare:66 | ||||
chr11:67303356-67303615 | Rare:70 | ||||
chr11:67317807-67317890 | Rare:22 | ||||
chr11:67401789-67402075 | Common:3; Rare:103 | ||||
chr11:67428336-67428537 | Rare:69 | ||||
chr11:67443458-67443598 | Common:1; Rare:51 | ||||
chr11:67452374-67452439 | Rare:25 | ||||
chr11:67482941-67483148 | Rare:45; Clinvar:1; Clinvar (benign):2 | ||||
chr11:67508635-67508778 | Common:3; Rare:52 | ||||
chr11:67583637-67583864 | Common:1; Rare:75 | ||||
chr11:68030433-68030744 | Common:3; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
chr11:68271881-68272102 | Common:2; Rare:94 | ||||
chr11:68903791-68903943 | Common:4; Rare:69; Clinvar (benign):6 | ||||
chr11:69675303-69675503 | Rare:54 | ||||
chr11:70078391-70078659 | Rare:73 |