| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35114474-35115106 | Common:3; Rare:247 | ||||
| chr19:35124430-35124830 | Common:3; Rare:85 | ||||
| chr19:35213860-35214250 | Rare:66 | ||||
| chr19:35267910-35268233 | Common:13; Rare:200 | ||||
| chr19:35317460-35317886 | Common:3; Rare:146 | ||||
| chr19:35388340-35388810 | Common:5; Rare:104 | ||||
| chr19:35420360-35420670 | Common:1; Rare:58 | ||||
| chr19:35436290-35436860 | Common:5; Rare:105 | ||||
| chr19:35509240-35509530 | Common:4; Rare:117 | ||||
| chr19:35673229-35673748 | Common:9; Rare:545 | ||||
| chr19:35702310-35702745 | Common:11; Rare:240 | ||||
| chr19:35702836-35702991 | Rare:29 | ||||
| chr19:35716830-35717320 | Common:10; Rare:214 | ||||
| chr19:35719492-35719892 | Rare:186; Clinvar (pathogenic):1 | ||||
| chr19:35750242-35750642 | Rare:106 |