| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:24314690-24314960 | Rare:46 | ||||
| chr14:24429664-24429990 | Common:3; Rare:85 | ||||
| chr14:24430517-24430748 | Common:1; Rare:45 | ||||
| chr14:24442695-24443043 | Common:5; Rare:107 | ||||
| chr14:30622175-30622350 | Rare:61 | ||||
| chr14:31025638-31025652 | Rare:6 | ||||
| chr14:31420527-31420763 | Common:3; Rare:71 | ||||
| chr14:34875336-34875582 | Common:1; Rare:81 | ||||
| chr14:34982501-34982590 | Common:1; Rare:39 | ||||
| chr14:35046079-35046466 | Common:2; Rare:126 | ||||
| chr14:35122232-35122695 | Common:2; Rare:132 | ||||
| chr14:35292188-35292493 | Common:5; Rare:110; Clinvar:1 | ||||
| chr14:35403688-35403950 | Common:1; Rare:91; Clinvar:1; Clinvar (benign):3 | ||||
| chr14:35403958-35404323 | Common:3; Rare:123 | ||||
| chr14:35404417-35404767 | Common:3; Rare:124; Clinvar:1; Clinvar (benign):5 |