| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75427930-75428237 | Rare:70 | ||||
| chr14:75660829-75661502 | Common:7; Rare:174 | ||||
| chr14:77097914-77098354 | Rare:144 | ||||
| chr14:77320862-77321094 | Rare:70; Clinvar:1 | ||||
| chr14:77377053-77377415 | Common:2; Rare:106 | ||||
| chr14:77457550-77457876 | Common:1; Rare:97 | ||||
| chr14:77457997-77458263 | Rare:62 | ||||
| chr14:77707988-77708152 | Common:2; Rare:89 | ||||
| chr14:81220596-81220633 | Rare:4 | ||||
| chr14:81220670-81221051 | Common:3; Rare:141 | ||||
| chr14:85530033-85530169 | Common:1; Rare:31 | ||||
| chr14:88824348-88824728 | Common:2; Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
| chr14:89417156-89417326 | Rare:44 | ||||
| chr14:89619119-89619260 | Common:1; Rare:53 | ||||
| chr14:89954661-89954968 | Rare:93 |