| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49598731-49599029 | Common:1; Rare:108 | ||||
| chr14:49620563-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
| chr14:49892898-49893136 | Rare:102 | ||||
| chr14:50312207-50312374 | Rare:64 | ||||
| chr14:50532485-50532757 | Common:3; Rare:88 | ||||
| chr14:50668340-50668560 | Common:4; Rare:87 | ||||
| chr14:50944350-50944541 | Common:2; Rare:77; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr14:51239977-51240291 | Common:2; Rare:101 | ||||
| chr14:51488586-51488835 | Common:1; Rare:45 | ||||
| chr14:51488865-51489206 | Common:1; Rare:63 | ||||
| chr14:51651613-51651934 | Common:4; Rare:82 | ||||
| chr14:52695482-52695841 | Common:1; Rare:104 | ||||
| chr14:52707045-52707271 | Common:1; Rare:100 | ||||
| chr14:52729851-52730237 | Common:2; Rare:121 | ||||
| chr14:52791427-52791873 | Common:2; Rare:141 |