| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50668277-50668560 | Common:4; Rare:105 | ||||
| chr14:50766465-50766655 | Common:1; Rare:30 | ||||
| chr14:50944257-50944600 | Common:5; Rare:120; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr14:51240149-51240421 | Rare:115 | ||||
| chr14:51554475-51554692 | Rare:42 | ||||
| chr14:51651409-51651460 | Rare:20 | ||||
| chr14:51651549-51652159 | Common:6; Rare:164 | ||||
| chr14:51989368-51989697 | Common:2; Rare:107 | ||||
| chr14:52069000-52069215 | Common:2; Rare:49 | ||||
| chr14:52707045-52707267 | Common:1; Rare:99 | ||||
| chr14:52729905-52730237 | Common:2; Rare:110 | ||||
| chr14:52791203-52791294 | Rare:18 | ||||
| chr14:52791421-52791895 | Common:3; Rare:149 | ||||
| chr14:52951002-52951442 | Common:4; Rare:157 | ||||
| chr14:53152381-53152433 | Rare:19 |