| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:54488920-54489174 | Common:2; Rare:114 | ||||
| chr14:54509603-54509969 | Common:9; Rare:185 | ||||
| chr14:54566560-54566850 | Rare:137 | ||||
| chr14:54566950-54567300 | Rare:123 | ||||
| chr14:54902030-54902430 | Common:4; Rare:226; Clinvar:4; Clinvar (pathogenic):5 | ||||
| chr14:54902667-54902964 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):4 | ||||
| chr14:55026965-55027322 | Common:4; Rare:171 | ||||
| chr14:55027350-55027650 | Common:2; Rare:78 | ||||
| chr14:55051442-55051776 | Rare:279 | ||||
| chr14:55051914-55052332 | Common:4; Rare:195 | ||||
| chr14:55129087-55129409 | Common:2; Rare:147 | ||||
| chr14:55191474-55191814 | Common:10; Rare:148 | ||||
| chr14:55271420-55272078 | Common:7; Rare:239 | ||||
| chr14:55411776-55411970 | Common:4; Rare:179 | ||||
| chr14:55580031-55580558 | Common:8; Rare:268 |