| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:102086990-102087338 | Common:8; Rare:266 | ||||
| chr14:102139200-102139470 | Rare:183 | ||||
| chr14:102139671-102139923 | Rare:172 | ||||
| chr14:102305115-102305358 | Common:2; Rare:137 | ||||
| chr14:102316870-102317310 | Common:19; Rare:378 | ||||
| chr14:102319625-102319799 | Common:2; Rare:96 | ||||
| chr14:102362835-102363115 | Rare:226 | ||||
| chr14:102508440-102508750 | Common:4; Rare:97 | ||||
| chr14:102509589-102510201 | Common:3; Rare:213 | ||||
| chr14:102591918-102592318 | Common:9; Rare:241 | ||||
| chr14:102592330-102592682 | Common:2; Rare:261 | ||||
| chr14:102776920-102777510 | Common:10; Rare:192 | ||||
| chr14:102922690-102923170 | Common:6; Rare:295; Clinvar (pathogenic):1 | ||||
| chr14:103057493-103057884 | Common:9; Rare:335 | ||||
| chr14:103333894-103334344 | Common:7; Rare:328 |