Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:31963986-31964242 | Common:2; Rare:43 | ||||
chr22:32204721-32205227 | Common:4; Rare:102 | ||||
chr22:32269564-32269770 | Common:2; Rare:39 | ||||
chr22:32504337-32504525 | Common:2; Rare:36 | ||||
chr22:33921051-33921320 | Common:1; Rare:93 | ||||
chr22:35761200-35761432 | Rare:64 | ||||
chr22:35836383-35836544 | Rare:40 | ||||
chr22:35838689-35839000 | Common:2; Rare:46 | ||||
chr22:36329540-36329779 | Rare:47 | ||||
chr22:36520483-36520684 | Rare:46 | ||||
chr22:37061493-37061511 | Rare:11 | ||||
chr22:37417872-37418110 | Rare:42 | ||||
chr22:38839680-38839945 | Common:1; Rare:44 | ||||
chr22:40179166-40179458 | Common:2; Rare:53 | ||||
chr22:41092836-41092899 | Rare:20; Clinvar:1; Clinvar (benign):1 |