| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38930742-38930992 | Common:3; Rare:65; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39125558-39125822 | Rare:64 | ||||
| chr19:39391045-39391431 | Common:1; Rare:158 | ||||
| chr19:39406738-39406894 | Rare:72 | ||||
| chr19:39435888-39436167 | Common:5; Rare:107 | ||||
| chr19:39846335-39846473 | Common:1; Rare:62 | ||||
| chr19:39970986-39971196 | Common:2; Rare:56 | ||||
| chr19:40056150-40056266 | Rare:15 | ||||
| chr19:40090873-40091014 | Common:1; Rare:38 | ||||
| chr19:40285243-40285520 | Common:1; Rare:103 | ||||
| chr19:40348393-40348724 | Common:4; Rare:105 | ||||
| chr19:40377800-40378060 | Common:2; Rare:102; Clinvar (benign):1 | ||||
| chr19:40413356-40413521 | Rare:48 | ||||
| chr19:40576696-40576900 | Common:3; Rare:59 | ||||
| chr19:40715074-40715167 | Rare:27 |