Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69398234-69398399 | Rare:71 | ||||
chr14:69398582-69398703 | Rare:28 | ||||
chr14:69611480-69611765 | Common:1; Rare:94 | ||||
chr14:70359607-70359836 | Common:1; Rare:44 | ||||
chr14:70417023-70417149 | Rare:32 | ||||
chr14:73058297-73058595 | Common:3; Rare:93 | ||||
chr14:73787124-73787369 | Common:2; Rare:86 | ||||
chr14:73886789-73886903 | Common:1; Rare:39 | ||||
chr14:73950163-73950333 | Common:3; Rare:76; Clinvar (benign):1 | ||||
chr14:74019263-74019441 | Common:1; Rare:68 | ||||
chr14:74493570-74493770 | Common:3; Rare:76; Clinvar (benign):4 | ||||
chr14:74713077-74713222 | Rare:71 | ||||
chr14:75002741-75003025 | Common:1; Rare:99; Clinvar:2; Clinvar (pathogenic):1 | ||||
chr14:75069355-75069609 | Common:1; Rare:69 | ||||
chr14:75127001-75127154 | Common:1; Rare:55 |