| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77097701-77098550 | Common:2; Rare:564 | ||||
| chr14:77098591-77099916 | Common:15; Rare:429 | ||||
| chr14:77139942-77140873 | Common:5; Rare:242 | ||||
| chr14:77140990-77141450 | Common:1; Rare:116 | ||||
| chr14:77141610-77142360 | Common:4; Rare:191 | ||||
| chr14:77181549-77181903 | Common:4; Rare:122 | ||||
| chr14:77301014-77301414 | Common:3; Rare:160; Clinvar:15; Clinvar (pathogenic):4 | ||||
| chr14:77320184-77320521 | Common:6; Rare:152; Clinvar:8; Clinvar (benign):5; Clinvar (pathogenic):6 | ||||
| chr14:77320663-77321622 | Common:28; Rare:925; Clinvar:11; Clinvar (benign):8 | ||||
| chr14:77376265-77376872 | Common:6; Rare:220 | ||||
| chr14:77376953-77377459 | Common:11; Rare:376 | ||||
| chr14:77457436-77457892 | Common:11; Rare:373 | ||||
| chr14:77457929-77458254 | Rare:192 | ||||
| chr14:77498794-77498949 | Rare:51 | ||||
| chr14:77616546-77617163 | Common:9; Rare:448; Clinvar:9; Clinvar (benign):15 |