| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39342404-39342518 | Common:2; Rare:42 | ||||
| chr19:39390974-39391418 | Common:1; Rare:169 | ||||
| chr19:39445478-39445813 | Common:2; Rare:90 | ||||
| chr19:39480763-39480931 | Common:2; Rare:88; Clinvar (pathogenic):1 | ||||
| chr19:39846335-39846470 | Common:1; Rare:60 | ||||
| chr19:39970935-39971196 | Common:4; Rare:73 | ||||
| chr19:40056157-40056243 | Rare:14 | ||||
| chr19:40348356-40348739 | Common:4; Rare:125 | ||||
| chr19:40425949-40426147 | Common:2; Rare:75 | ||||
| chr19:40750477-40750763 | Common:2; Rare:71 | ||||
| chr19:40751096-40751220 | Common:1; Rare:28 | ||||
| chr19:41218997-41219443 | Common:2; Rare:109 | ||||
| chr19:41310139-41310261 | Rare:47 | ||||
| chr19:41397332-41397604 | Common:4; Rare:71 |