| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:75982283-75982341 | Rare:14 | ||||
| chr14:75982471-75982646 | Common:2; Rare:34 | ||||
| chr14:75985673-75985818 | Rare:65; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr14:76151742-76152013 | Common:1; Rare:95 | ||||
| chr14:76761665-76761693 | Rare:4 | ||||
| chr14:76812209-76812253 | Rare:8 | ||||
| chr14:76812503-76812669 | Common:2; Rare:35 | ||||
| chr14:76812709-76813062 | Common:4; Rare:132 | ||||
| chr14:77028370-77028530 | Common:3; Rare:45 | ||||
| chr14:77028554-77029034 | Common:1; Rare:147 | ||||
| chr14:77097725-77098414 | Common:1; Rare:206 | ||||
| chr14:77181621-77181922 | Common:3; Rare:70 | ||||
| chr14:77320284-77320526 | Common:4; Rare:75; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr14:77320782-77321130 | Common:2; Rare:107; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:77321165-77321525 | Common:7; Rare:173 |