Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:81436431-81436618 | Common:1; Rare:73 | ||||
chr14:88562917-88563155 | Rare:107 | ||||
chr14:88824350-88824710 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):1 | ||||
chr14:89619106-89619249 | Common:1; Rare:48 | ||||
chr14:89954693-89954918 | Rare:61 | ||||
chr14:90331900-90332209 | Common:1; Rare:90 | ||||
chr14:90396973-90397254 | Common:5; Rare:127; Clinvar (benign):2 | ||||
chr14:91060308-91060426 | Common:1; Rare:58 | ||||
chr14:91060439-91060457 | Rare:7 | ||||
chr14:91060476-91060511 | Rare:12 | ||||
chr14:91114028-91114118 | Rare:34 | ||||
chr14:91114568-91114699 | Common:1; Rare:14 | ||||
chr14:91510239-91510631 | Common:1; Rare:127 | ||||
chr14:91836382-91836695 | Common:13; Rare:58 | ||||
chr14:92039792-92040192 | Common:3; Rare:102; Clinvar:7; Clinvar (benign):2 |