| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50831101-50831377 | Common:1; Rare:88 | ||||
| chr14:50944480-50944795 | Common:7; Rare:78; Clinvar (benign):1 | ||||
| chr14:51095039-51095442 | Common:4; Rare:160 | ||||
| chr14:51095475-51095710 | Rare:60 | ||||
| chr14:51239944-51240374 | Common:2; Rare:144 | ||||
| chr14:51240500-51240657 | Common:2; Rare:50 | ||||
| chr14:51651341-51651502 | Common:1; Rare:54 | ||||
| chr14:51651597-51652207 | Common:6; Rare:165 | ||||
| chr14:51652345-51652460 | Common:1; Rare:27 | ||||
| chr14:51860432-51860441 | |||||
| chr14:51860530-51860767 | Rare:67 | ||||
| chr14:51989310-51989651 | Common:2; Rare:108 | ||||
| chr14:51989787-51989815 | Rare:9 | ||||
| chr14:52069019-52069261 | Common:2; Rare:52 | ||||
| chr14:52069357-52069442 | Common:4; Rare:15 |