| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12666650-12666848 | Rare:83; Clinvar:4 | ||||
| chr19:12669363-12669823 | Common:5; Rare:168 | ||||
| chr19:12669909-12670006 | Rare:36 | ||||
| chr19:12681062-12681686 | Common:3; Rare:228 | ||||
| chr19:12681716-12682107 | Common:4; Rare:167; Clinvar (pathogenic):1 | ||||
| chr19:12696500-12696748 | Rare:105 | ||||
| chr19:12721678-12721850 | Rare:31 | ||||
| chr19:12721972-12722093 | Rare:25 | ||||
| chr19:12722096-12722482 | Common:1; Rare:61 | ||||
| chr19:12722485-12722891 | Common:4; Rare:79 | ||||
| chr19:12722970-12723088 | Rare:27 | ||||
| chr19:12723587-12724135 | Common:1; Rare:122 | ||||
| chr19:12734219-12734366 | Rare:38 | ||||
| chr19:12734548-12734910 | Common:1; Rare:129 | ||||
| chr19:12736822-12737298 | Common:2; Rare:110 |