| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42519227-42519304 | Rare:19 | ||||
| chr19:43205627-43205677 | Common:7; Rare:9 | ||||
| chr19:43465494-43465790 | Common:1; Rare:104 | ||||
| chr19:43527155-43527302 | Common:5; Rare:62; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43670129-43670309 | Common:2; Rare:43 | ||||
| chr19:43799824-43800151 | Common:1; Rare:56 | ||||
| chr19:44141505-44141636 | Common:1; Rare:18 | ||||
| chr19:44164834-44165141 | Common:1; Rare:75 | ||||
| chr19:44305001-44305091 | Rare:27 | ||||
| chr19:44643801-44643887 | Rare:26 | ||||
| chr19:44808948-44809136 | Rare:67 | ||||
| chr19:45038978-45039094 | Rare:40 | ||||
| chr19:45079174-45079279 | Rare:28 | ||||
| chr19:45406340-45406649 | Common:1; Rare:67 | ||||
| chr19:45692372-45692678 | Common:1; Rare:65 |