| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:69611462-69611769 | Common:1; Rare:101 | ||||
| chr14:70416998-70417175 | Rare:45 | ||||
| chr14:71320306-71320491 | Rare:57 | ||||
| chr14:71321776-71321819 | Common:1; Rare:9 | ||||
| chr14:72894094-72894260 | Common:4; Rare:59 | ||||
| chr14:72926148-72926524 | Common:6; Rare:95 | ||||
| chr14:73058301-73058595 | Common:3; Rare:92 | ||||
| chr14:73458504-73458870 | Common:5; Rare:96 | ||||
| chr14:73463555-73463766 | Common:1; Rare:37 | ||||
| chr14:73568908-73569292 | Common:1; Rare:77 | ||||
| chr14:73644900-73645034 | Common:2; Rare:37; Clinvar:2 | ||||
| chr14:73714376-73714499 | Common:1; Rare:44 | ||||
| chr14:73787175-73787379 | Common:2; Rare:75 | ||||
| chr14:73851773-73851974 | Common:4; Rare:69 | ||||
| chr14:73950059-73950323 | Common:6; Rare:112; Clinvar (benign):4 |