Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:37197819-37198048 | Common:2; Rare:78 | ||||
chr14:39103095-39103359 | Common:2; Rare:71 | ||||
chr14:39170272-39170471 | Common:3; Rare:64 | ||||
chr14:39175002-39175289 | Common:3; Rare:100 | ||||
chr14:39432420-39432612 | Common:6; Rare:63 | ||||
chr14:44961908-44962244 | Common:3; Rare:97 | ||||
chr14:45253186-45253294 | Rare:20 | ||||
chr14:49586322-49586772 | Common:1; Rare:238; Clinvar (benign):1 | ||||
chr14:49598731-49599014 | Common:1; Rare:104 | ||||
chr14:49620573-49620830 | Common:2; Rare:105; Clinvar:3 | ||||
chr14:49892909-49893125 | Rare:87 | ||||
chr14:50312215-50312324 | Rare:36 | ||||
chr14:50396874-50396976 | Common:1; Rare:25 | ||||
chr14:50532522-50532624 | Common:2; Rare:30 | ||||
chr14:50668349-50668560 | Common:4; Rare:85 |