Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:90828153-90828387 | Common:2; Rare:62 | ||||
chr14:92039221-92039504 | Common:1; Rare:57 | ||||
chr14:92071328-92071572 | Common:5; Rare:48 | ||||
chr14:96362844-96362881 | Rare:8 | ||||
chr14:100274749-100274777 | Rare:5 | ||||
chr14:100366542-100366586 | Rare:10 | ||||
chr14:101473656-101473856 | Common:1; Rare:27 | ||||
chr14:101477037-101477169 | Rare:19 | ||||
chr14:102029535-102029936 | Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
chr14:102083254-102083647 | Common:5; Rare:152 | ||||
chr14:102913394-102913434 | Common:1; Rare:5 | ||||
chr14:103694548-103694677 | Rare:21 | ||||
chr14:103694960-103695233 | Common:3; Rare:58 | ||||
chr14:103696082-103696181 | Common:6; Rare:26 | ||||
chr14:104688248-104688344 | Rare:32 |