| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77377046-77377190 | Common:2; Rare:99 | ||||
| chr14:77457518-77457884 | Common:2; Rare:219 | ||||
| chr14:77457997-77458253 | Rare:92 | ||||
| chr14:77498674-77499085 | Common:5; Rare:163 | ||||
| chr14:77498987-77499199 | Common:2; Rare:57 | ||||
| chr14:77616755-77617082 | Common:1; Rare:71; Clinvar (benign):2 | ||||
| chr14:77707988-77708131 | Common:2; Rare:144 | ||||
| chr14:77800051-77800163 | Rare:23 | ||||
| chr14:81220861-81221171 | Common:2; Rare:244 | ||||
| chr14:81221220-81221630 | Common:2; Rare:168 | ||||
| chr14:81436382-81436625 | Common:6; Rare:170 | ||||
| chr14:88562922-88563086 | Rare:149 | ||||
| chr14:88563400-88563700 | Rare:220; Clinvar (benign):2 | ||||
| chr14:89417005-89417442 | Common:6; Rare:226 | ||||
| chr14:89619085-89619261 | Common:2; Rare:118 |