Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:67248401-67248568 | Common:1; Rare:43 | ||||
chr16:67248833-67248990 | Rare:33 | ||||
chr16:67279390-67279574 | Rare:53 | ||||
chr16:67416425-67416564 | Rare:46 | ||||
chr16:67430432-67430628 | Rare:34 | ||||
chr16:67430958-67431327 | Common:1; Rare:80; Clinvar (pathogenic):1 | ||||
chr16:67481057-67481404 | Common:1; Rare:127 | ||||
chr16:67528691-67528878 | Rare:56 | ||||
chr16:67537350-67537514 | Common:2; Rare:34 | ||||
chr16:67562457-67562721 | Common:1; Rare:88 | ||||
chr16:67660202-67660352 | Rare:78; Clinvar:2; Clinvar (benign):2 | ||||
chr16:67660736-67661079 | Common:2; Rare:119 | ||||
chr16:67663804-67664109 | Common:4; Rare:103 | ||||
chr16:67666229-67666353 | Common:1; Rare:49 | ||||
chr16:67666708-67666845 | Rare:30 |