| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50116551-50116641 | Rare:49 | ||||
| chr14:50312207-50312374 | Rare:64 | ||||
| chr14:50396879-50396991 | Common:1; Rare:28 | ||||
| chr14:50532463-50532751 | Common:2; Rare:91 | ||||
| chr14:50668340-50668563 | Common:4; Rare:89 | ||||
| chr14:50944393-50944620 | Common:4; Rare:78; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51554475-51554696 | Rare:43 | ||||
| chr14:51651666-51652040 | Common:4; Rare:106 | ||||
| chr14:51989374-51989642 | Common:2; Rare:86 | ||||
| chr14:52068963-52069253 | Common:2; Rare:70 | ||||
| chr14:52314095-52314376 | Common:1; Rare:77 | ||||
| chr14:52695518-52695809 | Common:1; Rare:77 | ||||
| chr14:52707099-52707300 | Common:1; Rare:78 | ||||
| chr14:52791437-52791766 | Common:1; Rare:113 | ||||
| chr14:52951172-52951442 | Common:3; Rare:110 |