Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:73886777-73886905 | Common:2; Rare:43 | ||||
chr14:73950130-73950323 | Common:4; Rare:79; Clinvar (benign):2 | ||||
chr14:74019248-74019436 | Common:1; Rare:74 | ||||
chr14:74084403-74084638 | Common:2; Rare:60 | ||||
chr14:74493568-74493777 | Common:3; Rare:78; Clinvar (benign):4 | ||||
chr14:74713036-74713213 | Rare:100 | ||||
chr14:74763248-74763404 | Rare:58 | ||||
chr14:74881840-74881970 | Rare:61 | ||||
chr14:75002710-75002972 | Common:1; Rare:86; Clinvar:2 | ||||
chr14:75126978-75127116 | Rare:53 | ||||
chr14:75660813-75661314 | Common:4; Rare:121 | ||||
chr14:76151794-76151982 | Rare:64 | ||||
chr14:77320838-77321056 | Rare:64; Clinvar:1 | ||||
chr14:77377022-77377425 | Common:3; Rare:122 | ||||
chr14:77457555-77457787 | Common:1; Rare:73 |