| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49767997-49768257 | Common:2; Rare:100 | ||||
| chr14:49852736-49852847 | Common:2; Rare:52 | ||||
| chr14:49892909-49893105 | Rare:79 | ||||
| chr14:50116541-50116626 | Rare:51 | ||||
| chr14:50312146-50312376 | Rare:101 | ||||
| chr14:50532442-50532798 | Common:4; Rare:110 | ||||
| chr14:50559889-50560026 | Rare:29 | ||||
| chr14:50561080-50561234 | Rare:26 | ||||
| chr14:50668329-50668560 | Common:4; Rare:88 | ||||
| chr14:50944378-50944562 | Common:4; Rare:72; Clinvar:1; Clinvar (benign):2 | ||||
| chr14:51095063-51095297 | Common:4; Rare:89 | ||||
| chr14:51240021-51240295 | Common:2; Rare:98 | ||||
| chr14:51651758-51651950 | Common:4; Rare:50 | ||||
| chr14:51860538-51860781 | Rare:68 | ||||
| chr14:51989380-51989671 | Common:2; Rare:94 |