| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:94114691-94114899 | Rare:46 | ||||
| chr14:94390633-94390923 | Common:1; Rare:72 | ||||
| chr14:95105738-95106072 | Common:2; Rare:61; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:95157323-95157716 | Common:4; Rare:132; Clinvar:2; Clinvar (benign):1 | ||||
| chr14:95158003-95158025 | Common:1; Rare:5 | ||||
| chr14:95534535-95534683 | Common:2; Rare:63 | ||||
| chr14:95534729-95535075 | Common:4; Rare:111; Clinvar (benign):3 | ||||
| chr14:96256263-96256301 | Common:1; Rare:8 | ||||
| chr14:96363290-96363559 | Common:1; Rare:91 | ||||
| chr14:96502291-96502614 | Common:1; Rare:132 | ||||
| chr14:96560624-96560674 | Common:1; Rare:14 | ||||
| chr14:99271478-99271881 | Common:1; Rare:71 | ||||
| chr14:99480729-99480916 | Common:2; Rare:77 | ||||
| chr14:99580160-99580226 | Rare:13 | ||||
| chr14:99604151-99604489 | Common:3; Rare:104 |