| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:45134164-45134263 | Common:1; Rare:33 | ||||
| chr14:45134334-45134760 | Rare:153 | ||||
| chr14:45135716-45136047 | Common:1; Rare:83; Clinvar:1 | ||||
| chr14:45136158-45136249 | Rare:29; Clinvar:2 | ||||
| chr14:45253039-45253496 | Common:1; Rare:137 | ||||
| chr14:45253522-45253660 | Common:1; Rare:51 | ||||
| chr14:45254009-45254112 | Rare:23 | ||||
| chr14:49585857-49586173 | Common:1; Rare:100; Clinvar (pathogenic):1 | ||||
| chr14:49586348-49586853 | Common:1; Rare:264 | ||||
| chr14:49598241-49598495 | Common:1; Rare:67 | ||||
| chr14:49598553-49598777 | Common:3; Rare:101 | ||||
| chr14:49598811-49599078 | Common:1; Rare:92 | ||||
| chr14:49599103-49599408 | Rare:88 | ||||
| chr14:49620260-49620444 | Rare:49 | ||||
| chr14:49620549-49620903 | Common:2; Rare:134; Clinvar:4 |