| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77457958-77458145 | Rare:51 | ||||
| chr14:77707991-77708178 | Common:2; Rare:98 | ||||
| chr14:77761117-77761483 | Common:3; Rare:112 | ||||
| chr14:80212174-80212348 | Common:1; Rare:25 | ||||
| chr14:81220861-81221131 | Common:1; Rare:130 | ||||
| chr14:81221275-81221495 | Common:1; Rare:62 | ||||
| chr14:81324124-81324286 | Common:1; Rare:25 | ||||
| chr14:85530030-85530208 | Common:1; Rare:39 | ||||
| chr14:88824325-88824716 | Common:2; Rare:112; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89619097-89619260 | Common:1; Rare:58 | ||||
| chr14:89954693-89954950 | Rare:72 | ||||
| chr14:89955641-89955962 | Common:10; Rare:88; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:90331913-90332194 | Common:1; Rare:79 | ||||
| chr14:90396870-90397232 | Common:5; Rare:171; Clinvar (benign):2 | ||||
| chr14:91060583-91060926 | Common:3; Rare:102 |