| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:44386070-44386158 | Rare:20 | ||||
| chr14:44480596-44480724 | Common:2; Rare:24 | ||||
| chr14:44799428-44799664 | Common:1; Rare:69 | ||||
| chr14:44912143-44912495 | Common:4; Rare:106 | ||||
| chr14:44912762-44913048 | Common:4; Rare:92 | ||||
| chr14:45232789-45232975 | Common:1; Rare:41 | ||||
| chr14:46063974-46064160 | Rare:36 | ||||
| chr14:46820379-46820503 | Common:1; Rare:54 | ||||
| chr14:47243233-47243392 | Rare:34 | ||||
| chr14:47627489-47627718 | Common:2; Rare:48 | ||||
| chr14:47938983-47939114 | Common:1; Rare:26 | ||||
| chr14:48194045-48194168 | Rare:52 | ||||
| chr14:48253107-48253187 | Rare:11 | ||||
| chr14:49550289-49550438 | Common:1; Rare:30 | ||||
| chr14:49633891-49634094 | Common:1; Rare:87; Clinvar:12; Clinvar (benign):4; Clinvar (pathogenic):2 |