| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77321581-77321929 | Common:4; Rare:93 | ||||
| chr14:77376638-77376855 | Common:1; Rare:47 | ||||
| chr14:77376926-77377223 | Common:4; Rare:87 | ||||
| chr14:77377355-77377454 | Rare:40 | ||||
| chr14:77457361-77457431 | Rare:27 | ||||
| chr14:77457436-77457890 | Common:6; Rare:136 | ||||
| chr14:77457961-77458156 | Rare:55 | ||||
| chr14:77458505-77458585 | Common:1; Rare:21 | ||||
| chr14:77498231-77498293 | Rare:13 | ||||
| chr14:77498641-77499200 | Common:4; Rare:156 | ||||
| chr14:77616561-77616724 | Common:2; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:77616739-77617152 | Common:1; Rare:98; Clinvar (benign):2 | ||||
| chr14:77707566-77707772 | Common:1; Rare:56 | ||||
| chr14:77707981-77708131 | Common:1; Rare:79 | ||||
| chr14:77760438-77760591 | Common:1; Rare:27 |