| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:76762648-76762972 | Rare:106 | ||||
| chr14:77097947-77098354 | Rare:132 | ||||
| chr14:77320824-77321097 | Rare:86; Clinvar:2 | ||||
| chr14:77376976-77377411 | Common:5; Rare:126 | ||||
| chr14:77457550-77457876 | Common:1; Rare:97 | ||||
| chr14:77457977-77458181 | Rare:57 | ||||
| chr14:77707979-77708117 | Rare:68 | ||||
| chr14:77761113-77761204 | Rare:43 | ||||
| chr14:81220861-81221077 | Common:1; Rare:102 | ||||
| chr14:81221275-81221378 | Rare:16 | ||||
| chr14:88824348-88824708 | Common:2; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:89619097-89619242 | Common:1; Rare:46 | ||||
| chr14:89954689-89954943 | Rare:70 | ||||
| chr14:90331918-90332188 | Common:1; Rare:74 | ||||
| chr14:90396875-90397097 | Common:2; Rare:116 |