Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:75126978-75127104 | Rare:45 | ||||
chr14:75660800-75661055 | Rare:66 | ||||
chr14:75661183-75661334 | Common:2; Rare:41 | ||||
chr14:77377055-77377415 | Common:2; Rare:104 | ||||
chr14:77457556-77457844 | Common:1; Rare:89 | ||||
chr14:77708000-77708111 | Rare:53 | ||||
chr14:77761126-77761407 | Common:2; Rare:85 | ||||
chr14:85530024-85530145 | Common:1; Rare:25 | ||||
chr14:88824326-88824716 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
chr14:92040031-92040192 | Common:2; Rare:42; Clinvar (benign):1 | ||||
chr14:92121658-92121985 | Common:4; Rare:109 | ||||
chr14:93184837-93185004 | Rare:56 | ||||
chr14:93206994-93207284 | Common:2; Rare:143 | ||||
chr14:93430626-93430949 | Rare:56 | ||||
chr14:94081141-94081341 | Common:4; Rare:67 |