| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41364128-41364317 | Rare:58 | ||||
| chr19:41397558-41397859 | Common:7; Rare:107; Clinvar (benign):5 | ||||
| chr19:41860070-41860466 | Common:5; Rare:154; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41884132-41884452 | Rare:80 | ||||
| chr19:41959276-41959459 | Common:1; Rare:59 | ||||
| chr19:42075766-42076191 | Common:5; Rare:124 | ||||
| chr19:42217702-42217863 | Rare:61 | ||||
| chr19:42220108-42220358 | Common:2; Rare:66 | ||||
| chr19:42268254-42268557 | Rare:59 | ||||
| chr19:42302388-42302570 | Rare:47 | ||||
| chr19:42528394-42528563 | Common:3; Rare:43 | ||||
| chr19:43527158-43527310 | Common:5; Rare:60; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575459-43575834 | Common:2; Rare:97 | ||||
| chr19:43596051-43596465 | Common:3; Rare:126 | ||||
| chr19:43670158-43670316 | Common:2; Rare:37 |