| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40348364-40348715 | Common:4; Rare:110 | ||||
| chr19:40425990-40426147 | Common:1; Rare:45 | ||||
| chr19:40465680-40466098 | Common:3; Rare:133 | ||||
| chr19:40750488-40750714 | Common:2; Rare:62 | ||||
| chr19:40751064-40751259 | Common:1; Rare:56 | ||||
| chr19:41219115-41219443 | Common:1; Rare:87 | ||||
| chr19:41364137-41364311 | Rare:53 | ||||
| chr19:41397332-41397821 | Common:11; Rare:148; Clinvar (benign):4 | ||||
| chr19:41860060-41860285 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:42075896-42076191 | Rare:79 | ||||
| chr19:42302310-42302570 | Rare:74 | ||||
| chr19:43205541-43205756 | Common:15; Rare:76 | ||||
| chr19:43575459-43575598 | Common:1; Rare:55 | ||||
| chr19:43670126-43670324 | Common:2; Rare:53 | ||||
| chr19:43754855-43755094 | Common:3; Rare:98 |