Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:74019263-74019428 | Common:1; Rare:64 | ||||
chr14:74493570-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713075-74713200 | Rare:64 | ||||
chr14:74881784-74881959 | Common:1; Rare:76 | ||||
chr14:75002701-75002947 | Common:1; Rare:79; Clinvar:2 | ||||
chr14:75127008-75127104 | Rare:26 | ||||
chr14:75660819-75660962 | Rare:36 | ||||
chr14:77377076-77377412 | Common:1; Rare:93 | ||||
chr14:77458007-77458121 | Rare:28 | ||||
chr14:77708000-77708161 | Common:2; Rare:88 | ||||
chr14:81220871-81221046 | Common:1; Rare:85 | ||||
chr14:81436457-81436595 | Rare:49 | ||||
chr14:88562907-88563084 | Rare:81 | ||||
chr14:90396870-90397078 | Common:2; Rare:115 | ||||
chr14:92040025-92040148 | Common:2; Rare:33; Clinvar (benign):1 |