| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:95157444-95157707 | Common:4; Rare:94 | ||||
| chr14:95534593-95534679 | Rare:28 | ||||
| chr14:96204732-96204889 | Common:2; Rare:55 | ||||
| chr14:96363333-96363552 | Common:1; Rare:71 | ||||
| chr14:96502286-96502460 | Rare:66 | ||||
| chr14:100375394-100375684 | Common:2; Rare:42 | ||||
| chr14:100376269-100376535 | Common:3; Rare:86 | ||||
| chr14:102139662-102139942 | Rare:98 | ||||
| chr14:102305124-102305308 | Common:1; Rare:60 | ||||
| chr14:102362862-102363092 | Rare:103 | ||||
| chr14:103333978-103334246 | Rare:110 | ||||
| chr14:103334658-103334910 | Common:2; Rare:109 | ||||
| chr14:103522828-103522954 | Rare:40 | ||||
| chr14:103562624-103563217 | Common:11; Rare:247; Clinvar:1; Clinvar (benign):9 | ||||
| chr14:103715466-103715847 | Common:1; Rare:122 |