| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5903635-5903841 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):5 | ||||
| chr19:5978062-5978418 | Common:3; Rare:137 | ||||
| chr19:6110471-6110817 | Common:2; Rare:103 | ||||
| chr19:6381384-6381853 | Common:5; Rare:202 | ||||
| chr19:6393371-6393577 | Common:2; Rare:61 | ||||
| chr19:6464371-6464593 | Common:1; Rare:53 | ||||
| chr19:6530897-6531037 | Common:3; Rare:63 | ||||
| chr19:6737227-6737511 | Common:5; Rare:79 | ||||
| chr19:7069665-7069739 | Common:1; Rare:22 | ||||
| chr19:7394883-7395218 | Common:6; Rare:92 | ||||
| chr19:7489008-7489135 | Common:1; Rare:63 | ||||
| chr19:7515978-7516139 | Rare:37 | ||||
| chr19:7533861-7534238 | Common:4; Rare:98; Clinvar (benign):2 | ||||
| chr19:7535631-7535760 | Common:2; Rare:43 | ||||
| chr19:7629530-7629848 | Common:5; Rare:114; Clinvar (benign):2; Clinvar (pathogenic):1 |