| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:23154256-23154950 | Common:18; Rare:313 | ||||
| chr14:23155004-23155404 | Common:4; Rare:164 | ||||
| chr14:23155315-23155526 | Common:4; Rare:81 | ||||
| chr14:23184960-23185461 | Common:8; Rare:131 | ||||
| chr14:23285804-23286456 | Common:7; Rare:719 | ||||
| chr14:23286511-23286911 | Common:2; Rare:96 | ||||
| chr14:23299618-23300018 | Common:4; Rare:82 | ||||
| chr14:23300497-23300973 | Common:2; Rare:171 | ||||
| chr14:23301029-23302859 | Common:33; Rare:1833 | ||||
| chr14:23302760-23303183 | Common:4; Rare:258 | ||||
| chr14:23306524-23306968 | Common:6; Rare:391 | ||||
| chr14:23320458-23320858 | Common:5; Rare:82 | ||||
| chr14:23320828-23321562 | Common:16; Rare:795; Clinvar:4; Clinvar (pathogenic):5 | ||||
| chr14:23321703-23322150 | Common:9; Rare:391 | ||||
| chr14:23322113-23322439 | Rare:126 |