Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:45253165-45253312 | Rare:37 | ||||
chr14:49586332-49586629 | Common:1; Rare:137 | ||||
chr14:49620573-49620797 | Common:2; Rare:87 | ||||
chr14:50312100-50312329 | Rare:95; Clinvar:1; Clinvar (benign):1 | ||||
chr14:51989374-51989626 | Common:2; Rare:77 | ||||
chr14:53953380-53953665 | Common:2; Rare:79 | ||||
chr14:53956713-53957070 | Rare:86; Clinvar:1 | ||||
chr14:55027059-55027283 | Common:2; Rare:61 | ||||
chr14:55129115-55129279 | Common:1; Rare:48 | ||||
chr14:55191538-55191768 | Common:5; Rare:56 | ||||
chr14:55411826-55411942 | Common:2; Rare:55 | ||||
chr14:55580108-55580285 | Common:2; Rare:79 | ||||
chr14:57268825-57269037 | Common:2; Rare:69 | ||||
chr14:58244647-58244930 | Rare:92 | ||||
chr14:59484327-59484553 | Common:2; Rare:88 |