Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:88554950-88555110 | Common:2; Rare:58 | ||||
chr14:88562878-88563128 | Rare:119 | ||||
chr14:88563436-88563608 | Rare:75 | ||||
chr14:89417068-89417390 | Rare:86 | ||||
chr14:89618978-89618996 | Rare:5 | ||||
chr14:89619106-89619299 | Common:1; Rare:70 | ||||
chr14:89954555-89954970 | Common:3; Rare:139 | ||||
chr14:90331897-90332188 | Common:1; Rare:86 | ||||
chr14:90396870-90397221 | Common:5; Rare:166; Clinvar (benign):2 | ||||
chr14:90397597-90397706 | Common:1; Rare:51 | ||||
chr14:91060167-91060378 | Common:2; Rare:84 | ||||
chr14:91060574-91060686 | Rare:39 | ||||
chr14:91113857-91114105 | Rare:54 | ||||
chr14:91114305-91114683 | Common:1; Rare:57 | ||||
chr14:91417691-91417966 | Common:4; Rare:91 |