| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40404239-40404463 | Common:1; Rare:46 | ||||
| chr19:40410086-40410184 | Rare:16 | ||||
| chr19:40417096-40417327 | Common:1; Rare:54 | ||||
| chr19:40420806-40420910 | Common:1; Rare:22 | ||||
| chr19:40420919-40421492 | Common:4; Rare:115 | ||||
| chr19:40421519-40421563 | Rare:6 | ||||
| chr19:40424490-40424651 | Rare:21 | ||||
| chr19:40433799-40434156 | Common:1; Rare:92 | ||||
| chr19:40434159-40434232 | Common:2; Rare:11 | ||||
| chr19:40435330-40435606 | Common:2; Rare:39 | ||||
| chr19:40461762-40461955 | Common:1; Rare:34 | ||||
| chr19:40603545-40603832 | Common:1; Rare:46 | ||||
| chr19:40604006-40604190 | Rare:38 | ||||
| chr19:40605560-40605747 | Rare:71; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:40605801-40605947 | Common:4; Rare:31 |