Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:35402742-35403181 | Common:5; Rare:134; Clinvar (benign):4 | ||||
chr14:35404546-35404865 | Common:3; Rare:109; Clinvar:1; Clinvar (benign):4 | ||||
chr14:38256067-38256247 | Common:1; Rare:49 | ||||
chr14:39175029-39175315 | Common:4; Rare:102 | ||||
chr14:39267116-39267448 | Common:1; Rare:122 | ||||
chr14:39432420-39432618 | Common:6; Rare:66 | ||||
chr14:44961908-44962306 | Common:3; Rare:117 | ||||
chr14:45253088-45253310 | Rare:58 | ||||
chr14:49586347-49586776 | Common:1; Rare:230 | ||||
chr14:49598731-49598996 | Rare:98 | ||||
chr14:49620563-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
chr14:49693022-49693188 | Common:1; Rare:63 | ||||
chr14:49767548-49767625 | Common:1; Rare:35 | ||||
chr14:49829255-49829397 | Rare:47 | ||||
chr14:49892779-49893142 | Common:1; Rare:150 |