| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:49892648-49892862 | Common:5; Rare:59 | ||||
| chr14:49892864-49893576 | Common:4; Rare:255 | ||||
| chr14:50116298-50116342 | Rare:16 | ||||
| chr14:50116448-50116775 | Common:1; Rare:157 | ||||
| chr14:50230950-50231097 | Common:3; Rare:31 | ||||
| chr14:50231527-50231821 | Common:1; Rare:84 | ||||
| chr14:50231837-50232122 | Common:1; Rare:108 | ||||
| chr14:50312108-50312439 | Common:1; Rare:141; Clinvar:1; Clinvar (benign):1 | ||||
| chr14:50312465-50312764 | Common:9; Rare:98 | ||||
| chr14:50312773-50312910 | Rare:35 | ||||
| chr14:50312923-50313203 | Common:2; Rare:84 | ||||
| chr14:50321224-50321433 | Rare:47 | ||||
| chr14:50321474-50321563 | Common:1; Rare:24 | ||||
| chr14:50396271-50396410 | Common:1; Rare:27 | ||||
| chr14:50396691-50396942 | Common:5; Rare:80 |