| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:52314237-52314324 | Rare:32 | ||||
| chr14:52552444-52552892 | Common:1; Rare:139 | ||||
| chr14:52707045-52707249 | Common:1; Rare:91 | ||||
| chr14:52729827-52730256 | Common:2; Rare:130 | ||||
| chr14:52791422-52791785 | Common:2; Rare:117 | ||||
| chr14:52864558-52864782 | Common:1; Rare:60 | ||||
| chr14:52950993-52951429 | Common:4; Rare:153 | ||||
| chr14:53153132-53153490 | Common:4; Rare:127 | ||||
| chr14:53953424-53953577 | Common:1; Rare:49 | ||||
| chr14:54396711-54397073 | Common:2; Rare:101 | ||||
| chr14:54488833-54489106 | Common:3; Rare:88 | ||||
| chr14:54489157-54489227 | Common:1; Rare:13 | ||||
| chr14:54509627-54509968 | Common:5; Rare:123 | ||||
| chr14:54902819-54902963 | Rare:41; Clinvar (benign):1 | ||||
| chr14:55026709-55027617 | Common:4; Rare:200 |