| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37218145-37218264 | Rare:19 | ||||
| chr19:37317666-37317977 | Common:8; Rare:83 | ||||
| chr19:37467445-37467482 | Rare:8 | ||||
| chr19:37469280-37469392 | Common:1; Rare:36 | ||||
| chr19:37594753-37594917 | Rare:46 | ||||
| chr19:37779571-37779662 | Rare:21 | ||||
| chr19:38264812-38264908 | Rare:38 | ||||
| chr19:38374413-38374802 | Rare:143 | ||||
| chr19:38618902-38619240 | Common:3; Rare:102 | ||||
| chr19:38647372-38647785 | Common:3; Rare:138 | ||||
| chr19:38724076-38724469 | Rare:154; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:38831774-38832030 | Common:3; Rare:75 | ||||
| chr19:38899596-38900018 | Rare:123 | ||||
| chr19:38930737-38930996 | Common:3; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39156456-39156660 | Common:2; Rare:42 |