Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24232289-24232484 | Common:6; Rare:58 | ||||
chr14:24242258-24242413 | Rare:54; Clinvar:1; Clinvar (benign):1 | ||||
chr14:24255065-24255407 | Rare:118; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr14:24260650-24260929 | Common:1; Rare:81 | ||||
chr14:24299743-24299871 | Common:2; Rare:36 | ||||
chr14:24310026-24310164 | Rare:30 | ||||
chr14:24429861-24429974 | Rare:26 | ||||
chr14:24442670-24443023 | Common:5; Rare:114 | ||||
chr14:25049085-25049214 | Common:1; Rare:23 | ||||
chr14:31025636-31025664 | Rare:8 | ||||
chr14:31207458-31207911 | Common:2; Rare:147 | ||||
chr14:32076691-32077041 | Common:3; Rare:108 | ||||
chr14:34875264-34875344 | Rare:35 | ||||
chr14:34875348-34875647 | Common:1; Rare:89 | ||||
chr14:34982504-34982682 | Common:1; Rare:73 |