| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23094652-23094868 | Common:1; Rare:68 | ||||
| chr14:23095067-23095620 | Common:3; Rare:237 | ||||
| chr14:23095681-23095912 | Common:4; Rare:59 | ||||
| chr14:23286002-23286454 | Common:2; Rare:115 | ||||
| chr14:23286563-23286667 | Rare:21 | ||||
| chr14:23300691-23300777 | Rare:19 | ||||
| chr14:23301200-23301668 | Common:3; Rare:137 | ||||
| chr14:23301683-23302053 | Common:1; Rare:116 | ||||
| chr14:23302377-23302534 | Common:1; Rare:49 | ||||
| chr14:23302759-23303012 | Rare:49 | ||||
| chr14:23306591-23306996 | Common:1; Rare:87 | ||||
| chr14:23320845-23321116 | Common:3; Rare:58 | ||||
| chr14:23321188-23321658 | Common:2; Rare:141; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr14:23321787-23321935 | Common:1; Rare:37 | ||||
| chr14:23322271-23322436 | Rare:38 |