Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:48260515-48260713 | Common:3; Rare:58 | ||||
chr14:48260730-48260947 | Rare:57 | ||||
chr14:48262071-48262228 | Rare:36 | ||||
chr14:48264421-48264517 | Common:1; Rare:25 | ||||
chr14:48264776-48264922 | Common:4; Rare:46 | ||||
chr14:48267783-48267837 | Common:1; Rare:15 | ||||
chr14:48268061-48268120 | Rare:16 | ||||
chr14:49633557-49633612 | Rare:26; Clinvar:2; Clinvar (benign):1 | ||||
chr14:49633931-49634113 | Common:1; Rare:83; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr14:49634258-49634536 | Common:1; Rare:136; Clinvar:10; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr14:49862899-49863020 | Rare:45 | ||||
chr14:50458494-50458751 | Common:1; Rare:50 | ||||
chr14:50479316-50479666 | Common:3; Rare:59 | ||||
chr14:50670482-50670595 | Common:1; Rare:19 | ||||
chr14:50894269-50894308 | Common:1; Rare:6 |