| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36605263-36605347 | Rare:21 | ||||
| chr19:36687370-36687624 | Common:2; Rare:80 | ||||
| chr19:36772795-36772949 | Common:1; Rare:41 | ||||
| chr19:36916028-36916315 | Common:3; Rare:45 | ||||
| chr19:37078281-37078467 | Common:2; Rare:44 | ||||
| chr19:37172669-37172905 | Rare:43 | ||||
| chr19:37210529-37210734 | Common:2; Rare:44 | ||||
| chr19:37467177-37467519 | Common:2; Rare:99 | ||||
| chr19:37594740-37594910 | Rare:49 | ||||
| chr19:37907039-37907293 | Rare:57 | ||||
| chr19:37932464-37932616 | Common:1; Rare:33 | ||||
| chr19:38264253-38264706 | Common:6; Rare:115 | ||||
| chr19:38618912-38619246 | Common:3; Rare:100 | ||||
| chr19:38647362-38647763 | Common:3; Rare:134 | ||||
| chr19:38831768-38832061 | Common:4; Rare:83; Clinvar (benign):1 |