| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:50944350-50944546 | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51095063-51095297 | Common:4; Rare:89 | ||||
| chr14:51239996-51240287 | Common:2; Rare:95 | ||||
| chr14:51651611-51651964 | Common:4; Rare:95 | ||||
| chr14:51989374-51989666 | Common:2; Rare:93 | ||||
| chr14:52004107-52004238 | Common:1; Rare:51 | ||||
| chr14:52069000-52069226 | Common:2; Rare:50 | ||||
| chr14:52267551-52267735 | Common:2; Rare:64 | ||||
| chr14:52314284-52314388 | Common:1; Rare:31 | ||||
| chr14:52707045-52707238 | Common:1; Rare:86 | ||||
| chr14:52791437-52791757 | Common:1; Rare:110 | ||||
| chr14:52951171-52951436 | Common:3; Rare:108 | ||||
| chr14:53152371-53152516 | Rare:55 | ||||
| chr14:53956819-53956986 | Rare:41 | ||||
| chr14:54567016-54567177 | Rare:45 |