| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:103847964-103848021 | Rare:12 | ||||
| chr14:103921427-103921745 | Common:3; Rare:94 | ||||
| chr14:104049202-104049377 | Common:2; Rare:24 | ||||
| chr14:104689207-104689278 | Rare:13 | ||||
| chr14:104689427-104689673 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr14:104689981-104690184 | Common:1; Rare:50 | ||||
| chr14:104724069-104724412 | Common:3; Rare:115; Clinvar:1 | ||||
| chr14:104752617-104752738 | Common:1; Rare:29 | ||||
| chr14:104752938-104753277 | Common:3; Rare:132 | ||||
| chr14:104753714-104753922 | Common:3; Rare:87 | ||||
| chr14:104775174-104775286 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):3 | ||||
| chr14:104794593-104794820 | Common:1; Rare:41 | ||||
| chr14:104795330-104795431 | Rare:22 | ||||
| chr14:104795502-104795931 | Rare:107 | ||||
| chr14:104800478-104800689 | Common:2; Rare:55 |