| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43527147-43527308 | Common:5; Rare:65; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575478-43575693 | Common:1; Rare:70 | ||||
| chr19:43580460-43580572 | Common:4; Rare:25 | ||||
| chr19:43596073-43596450 | Common:2; Rare:116 | ||||
| chr19:43670129-43670339 | Common:2; Rare:53 | ||||
| chr19:43754850-43755102 | Common:3; Rare:100 | ||||
| chr19:43827216-43827433 | Common:2; Rare:45 | ||||
| chr19:43901765-43901882 | Common:1; Rare:24 | ||||
| chr19:44002787-44003006 | Common:4; Rare:60 | ||||
| chr19:44025222-44025439 | Common:1; Rare:51 | ||||
| chr19:44051759-44052072 | Common:2; Rare:71 | ||||
| chr19:44072035-44072173 | Common:1; Rare:33 | ||||
| chr19:44113129-44113519 | Common:4; Rare:82 | ||||
| chr19:44141472-44141643 | Common:2; Rare:23 | ||||
| chr19:44304992-44305167 | Rare:48 |