| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42075872-42076191 | Rare:84 | ||||
| chr19:42220112-42220349 | Common:2; Rare:66 | ||||
| chr19:42255128-42255387 | Common:1; Rare:93 | ||||
| chr19:42268254-42268570 | Rare:62 | ||||
| chr19:42528311-42528580 | Common:3; Rare:73; Clinvar:1 | ||||
| chr19:43527144-43527329 | Common:5; Rare:70; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43595985-43596440 | Common:5; Rare:144 | ||||
| chr19:43670129-43670344 | Common:2; Rare:54 | ||||
| chr19:43901782-43901882 | Rare:20 | ||||
| chr19:44002815-44003006 | Common:4; Rare:51 | ||||
| chr19:44072036-44072173 | Common:1; Rare:32 | ||||
| chr19:44113200-44113440 | Common:3; Rare:50 | ||||
| chr19:44141483-44141615 | Common:2; Rare:17 | ||||
| chr19:44164971-44165133 | Common:1; Rare:37 | ||||
| chr19:44305001-44305162 | Rare:42 |