| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75427748-75428147 | Rare:161 | ||||
| chr14:75428120-75428860 | Common:5; Rare:271 | ||||
| chr14:75522295-75522551 | Rare:117 | ||||
| chr14:75578464-75578706 | Common:4; Rare:81; Clinvar (benign):2 | ||||
| chr14:75578780-75579120 | Common:7; Rare:124; Clinvar:3; Clinvar (benign):7 | ||||
| chr14:75579360-75579860 | Common:5; Rare:125; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr14:75660760-75661491 | Common:9; Rare:309 | ||||
| chr14:75982489-75982697 | Common:1; Rare:45 | ||||
| chr14:75985667-75985830 | Rare:127; Clinvar:5; Clinvar (pathogenic):4 | ||||
| chr14:76151701-76152047 | Common:4; Rare:265 | ||||
| chr14:76152310-76152790 | Common:8; Rare:178 | ||||
| chr14:76761622-76761795 | Rare:56 | ||||
| chr14:76811960-76812440 | Common:3; Rare:140 | ||||
| chr14:76812703-76813079 | Common:6; Rare:253 | ||||
| chr14:77028368-77029202 | Common:8; Rare:512 |