| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49586327-49586772 | Common:1; Rare:237; Clinvar (benign):1 | ||||
| chr14:49598724-49599044 | Common:2; Rare:116 | ||||
| chr14:49620562-49620830 | Common:2; Rare:110; Clinvar:3 | ||||
| chr14:49688201-49688272 | Rare:26 | ||||
| chr14:49767580-49767688 | Common:1; Rare:38 | ||||
| chr14:49768036-49768261 | Common:2; Rare:87 | ||||
| chr14:49892892-49893142 | Rare:108 | ||||
| chr14:50116541-50116695 | Rare:75 | ||||
| chr14:50312155-50312376 | Rare:95 | ||||
| chr14:50396863-50397000 | Common:2; Rare:36 | ||||
| chr14:50532455-50532805 | Common:4; Rare:107 | ||||
| chr14:50561120-50561184 | Rare:12 | ||||
| chr14:50668295-50668560 | Common:4; Rare:98 | ||||
| chr14:50831018-50831343 | Common:1; Rare:108 | ||||
| chr14:50944287-50944657 | Common:6; Rare:128; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 |