| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49149376-49149576 | Common:1; Rare:70 | ||||
| chr19:49149614-49149986 | Common:1; Rare:81 | ||||
| chr19:49362324-49362473 | Rare:34 | ||||
| chr19:49451748-49452002 | Common:3; Rare:66 | ||||
| chr19:49453094-49453313 | Common:1; Rare:70 | ||||
| chr19:49453437-49453639 | Common:1; Rare:71 | ||||
| chr19:49487280-49487675 | Common:5; Rare:151 | ||||
| chr19:49496064-49496496 | Common:2; Rare:155 | ||||
| chr19:49527864-49528024 | Common:3; Rare:47 | ||||
| chr19:49580528-49580638 | Rare:41 | ||||
| chr19:49641796-49642240 | Rare:125 | ||||
| chr19:49665584-49666034 | Common:6; Rare:206; Clinvar (pathogenic):1 | ||||
| chr19:49851075-49851130 | Rare:20 | ||||
| chr19:49867212-49867368 | Common:1; Rare:54; Clinvar (benign):3 | ||||
| chr19:49867513-49867632 | Common:2; Rare:40; Clinvar:1 |