| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49892903-49893128 | Rare:92 | ||||
| chr14:50116488-50116724 | Common:1; Rare:130 | ||||
| chr14:50231547-50231665 | Common:1; Rare:29 | ||||
| chr14:50312034-50312380 | Common:2; Rare:147; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:50532494-50532782 | Common:3; Rare:96 | ||||
| chr14:50668291-50668482 | Common:1; Rare:68 | ||||
| chr14:50944359-50944595 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:50944699-50944784 | Common:1; Rare:20 | ||||
| chr14:51240019-51240432 | Common:2; Rare:149 | ||||
| chr14:51651454-51651471 | Rare:8 | ||||
| chr14:51651597-51651984 | Common:4; Rare:104 | ||||
| chr14:51860285-51860678 | Common:1; Rare:88 | ||||
| chr14:51989369-51989699 | Common:2; Rare:108 | ||||
| chr14:52004198-52004427 | Common:1; Rare:87 | ||||
| chr14:52068995-52069189 | Common:2; Rare:43 |