| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:81436429-81436581 | Rare:58 | ||||
| chr14:88562907-88563122 | Rare:101 | ||||
| chr14:89619093-89619262 | Common:1; Rare:60 | ||||
| chr14:89954656-89954950 | Rare:90 | ||||
| chr14:90397175-90397233 | Rare:20; Clinvar (benign):2 | ||||
| chr14:91114195-91114402 | Rare:37 | ||||
| chr14:91510254-91510577 | Common:1; Rare:104 | ||||
| chr14:92039829-92039929 | Rare:19 | ||||
| chr14:92040026-92040177 | Common:2; Rare:42; Clinvar (benign):1 | ||||
| chr14:92121658-92122005 | Common:4; Rare:120 | ||||
| chr14:92793988-92794408 | Rare:135 | ||||
| chr14:93184837-93185013 | Rare:61 | ||||
| chr14:93207038-93207294 | Common:2; Rare:128 | ||||
| chr14:94081118-94081376 | Common:6; Rare:81 | ||||
| chr14:95157422-95157707 | Common:4; Rare:100 |