| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42302329-42302403 | Rare:30 | ||||
| chr19:42405431-42405661 | Rare:58; Clinvar:1 | ||||
| chr19:42423543-42423806 | Common:4; Rare:86 | ||||
| chr19:42423941-42424066 | Rare:25 | ||||
| chr19:43527182-43527335 | Common:4; Rare:55; Clinvar:2; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr19:43575516-43575767 | Common:1; Rare:70 | ||||
| chr19:43596073-43596433 | Common:2; Rare:111 | ||||
| chr19:43670135-43670383 | Common:2; Rare:60 | ||||
| chr19:43827204-43827435 | Common:3; Rare:48 | ||||
| chr19:43901782-43901914 | Common:2; Rare:28 | ||||
| chr19:44002775-44002986 | Common:5; Rare:52 | ||||
| chr19:44051759-44052068 | Common:2; Rare:71 | ||||
| chr19:44071991-44072173 | Common:1; Rare:41 | ||||
| chr19:44113153-44113457 | Common:4; Rare:69 | ||||
| chr19:44141410-44141643 | Common:3; Rare:32 |