| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42423532-42423753 | Common:4; Rare:79 | ||||
| chr19:42442752-42443126 | Common:4; Rare:63 | ||||
| chr19:43527124-43527303 | Common:5; Rare:69; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575459-43575807 | Common:2; Rare:93 | ||||
| chr19:43580476-43580667 | Common:3; Rare:31 | ||||
| chr19:43595999-43596423 | Common:4; Rare:133 | ||||
| chr19:43596570-43596688 | Rare:37 | ||||
| chr19:43619572-43619659 | Common:1; Rare:30 | ||||
| chr19:43639794-43639926 | Common:1; Rare:44 | ||||
| chr19:43670111-43670402 | Common:2; Rare:70 | ||||
| chr19:43754838-43755088 | Common:3; Rare:99 | ||||
| chr19:43780923-43781150 | Rare:54 | ||||
| chr19:43827184-43827438 | Common:3; Rare:51 | ||||
| chr19:43901758-43901882 | Common:1; Rare:24 | ||||
| chr19:43935231-43935308 | Common:2; Rare:25 |