| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:35405040-35405261 | Common:1; Rare:42 | ||||
| chr14:35808200-35808371 | Rare:36 | ||||
| chr14:35808610-35808747 | Rare:38 | ||||
| chr14:35808818-35809023 | Common:1; Rare:52 | ||||
| chr14:35809096-35809311 | Common:2; Rare:55 | ||||
| chr14:35826120-35826534 | Common:1; Rare:110 | ||||
| chr14:35826609-35826954 | Common:1; Rare:110 | ||||
| chr14:36319623-36319652 | Rare:4 | ||||
| chr14:36320152-36320408 | Rare:46 | ||||
| chr14:36320538-36320848 | Common:5; Rare:99 | ||||
| chr14:36582102-36582720 | Common:5; Rare:176 | ||||
| chr14:36661669-36662005 | Rare:79; Clinvar:4 | ||||
| chr14:36662040-36662291 | Common:2; Rare:87 | ||||
| chr14:36662537-36662631 | Rare:21 | ||||
| chr14:36662746-36663084 | Common:5; Rare:84; Clinvar:3; Clinvar (pathogenic):3 |