Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:114077945-114078134 | Common:3; Rare:43 | ||||
chr14:32428242-32428382 | Rare:24 | ||||
chr14:49633938-49634079 | Common:1; Rare:57; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:49862635-49863044 | Common:1; Rare:186 | ||||
chr14:49868143-49868300 | Common:1; Rare:27 | ||||
chr14:58208716-58209018 | Common:1; Rare:60 | ||||
chr14:62117248-62117513 | Common:2; Rare:51 | ||||
chr14:68628383-68628679 | Common:2; Rare:69 | ||||
chr14:68795244-68795418 | Common:3; Rare:38 | ||||
chr14:69886145-69886166 | Rare:2 | ||||
chr14:73713468-73713521 | Common:1; Rare:6 | ||||
chr14:75258964-75259277 | Common:2; Rare:83 | ||||
chr14:75294182-75294446 | Common:1; Rare:71 | ||||
chr14:81170401-81170499 | Rare:27 | ||||
chr14:81219339-81219504 | Rare:37 |