| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:77377059-77377410 | Common:2; Rare:100 | ||||
| chr14:77457555-77457781 | Common:1; Rare:73 | ||||
| chr14:77707991-77708117 | Rare:59 | ||||
| chr14:81220871-81221082 | Common:1; Rare:100 | ||||
| chr14:88562951-88563075 | Rare:61 | ||||
| chr14:89954689-89954937 | Rare:69 | ||||
| chr14:92040031-92040140 | Common:2; Rare:28; Clinvar (benign):1 | ||||
| chr14:92121658-92121990 | Common:4; Rare:109 | ||||
| chr14:92794004-92794375 | Rare:113 | ||||
| chr14:93184856-93185020 | Rare:55 | ||||
| chr14:93206983-93207288 | Common:2; Rare:147 | ||||
| chr14:94081133-94081341 | Common:4; Rare:69 | ||||
| chr14:95534609-95534696 | Rare:27 | ||||
| chr14:96363369-96363552 | Common:1; Rare:62 | ||||
| chr14:96502301-96502460 | Rare:61 |