| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77320838-77321056 | Rare:64; Clinvar:1 | ||||
| chr14:77377038-77377410 | Common:3; Rare:109 | ||||
| chr14:77457536-77457877 | Common:1; Rare:103 | ||||
| chr14:77457987-77458166 | Rare:51 | ||||
| chr14:77707985-77708117 | Rare:63 | ||||
| chr14:81220861-81221069 | Common:1; Rare:100 | ||||
| chr14:81221285-81221418 | Common:1; Rare:29 | ||||
| chr14:85530033-85530184 | Common:1; Rare:34 | ||||
| chr14:87993010-87993260 | Common:4; Rare:127; Clinvar:13; Clinvar (benign):8; Clinvar (pathogenic):4 | ||||
| chr14:89619064-89619307 | Common:1; Rare:85 | ||||
| chr14:89954711-89954950 | Rare:64 | ||||
| chr14:90396866-90397232 | Common:5; Rare:174; Clinvar (benign):2 | ||||
| chr14:91113783-91114086 | Rare:64 | ||||
| chr14:91114592-91114671 | Common:1; Rare:6 | ||||
| chr14:91510226-91510631 | Common:1; Rare:131 |