| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:89954711-89954950 | Rare:64 | ||||
| chr14:90397181-90397232 | Rare:19; Clinvar (benign):2 | ||||
| chr14:91114043-91114112 | Rare:28 | ||||
| chr14:91510268-91510624 | Common:1; Rare:111 | ||||
| chr14:92040004-92040192 | Common:3; Rare:58; Clinvar:3; Clinvar (benign):2 | ||||
| chr14:92121667-92122000 | Common:4; Rare:111 | ||||
| chr14:92793943-92794408 | Rare:152 | ||||
| chr14:93184845-93185013 | Rare:56 | ||||
| chr14:93207016-93207294 | Common:2; Rare:138 | ||||
| chr14:94081141-94081371 | Common:4; Rare:73 | ||||
| chr14:95157422-95157685 | Common:4; Rare:93 | ||||
| chr14:95534609-95534692 | Rare:24 | ||||
| chr14:96363313-96363552 | Common:1; Rare:81 | ||||
| chr14:96502286-96502460 | Rare:66 | ||||
| chr14:99480769-99481013 | Common:2; Rare:95 |