| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:29606251-29606317 | Rare:27 | ||||
| chr19:29665252-29665504 | Common:4; Rare:89 | ||||
| chr19:29666360-29666619 | Common:2; Rare:43 | ||||
| chr19:29715033-29715313 | Common:1; Rare:105 | ||||
| chr19:31349210-31349551 | Common:4; Rare:115 | ||||
| chr19:32345543-32345718 | Common:1; Rare:49 | ||||
| chr19:32405560-32405817 | Common:1; Rare:106 | ||||
| chr19:32405916-32406175 | Common:2; Rare:86 | ||||
| chr19:32675124-32675413 | Common:4; Rare:96 | ||||
| chr19:32971903-32972277 | Common:4; Rare:107 | ||||
| chr19:33064867-33065058 | Common:1; Rare:65 | ||||
| chr19:33081126-33081255 | Common:1; Rare:55 | ||||
| chr19:33373554-33373845 | Common:2; Rare:93 | ||||
| chr19:33387954-33388206 | Common:2; Rare:93; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:33521730-33521964 | Common:1; Rare:79; Clinvar:5 |