Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:54487906-54487963 | Rare:9 | ||||
chr14:55103327-55103430 | Rare:22 | ||||
chr14:55581044-55581164 | Common:5; Rare:29 | ||||
chr14:56310753-56310954 | Common:2; Rare:37 | ||||
chr14:58260890-58260986 | Rare:31 | ||||
chr14:58266260-58266327 | Rare:16 | ||||
chr14:61562613-61563184 | Common:4; Rare:91 | ||||
chr14:61570596-61570672 | Rare:16 | ||||
chr14:61721506-61721822 | Common:1; Rare:61 | ||||
chr14:64223111-64223217 | Common:1; Rare:41; Clinvar:4; Clinvar (benign):2 | ||||
chr14:64442124-64442402 | Common:1; Rare:84; Clinvar (benign):1 | ||||
chr14:64454470-64454734 | Common:1; Rare:51 | ||||
chr14:67303413-67303543 | Common:1; Rare:30 | ||||
chr14:67376282-67376586 | Common:1; Rare:44 | ||||
chr14:67381417-67381630 | Common:3; Rare:35 |