| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:47778406-47778748 | Common:2; Rare:111 | ||||
| chr19:48170266-48170704 | Common:2; Rare:119 | ||||
| chr19:48445851-48446156 | Common:1; Rare:119 | ||||
| chr19:48551779-48552320 | Common:4; Rare:139 | ||||
| chr19:48615020-48615369 | Common:2; Rare:102 | ||||
| chr19:48619125-48619435 | Rare:102 | ||||
| chr19:48619468-48619665 | Rare:55 | ||||
| chr19:48624102-48624404 | Common:1; Rare:79 | ||||
| chr19:48695845-48696073 | Common:1; Rare:47 | ||||
| chr19:48872219-48872455 | Common:2; Rare:84 | ||||
| chr19:48899994-48900372 | Common:1; Rare:103 | ||||
| chr19:48933455-48933702 | Common:3; Rare:65 | ||||
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993188-48993914 | Common:9; Rare:258; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49085123-49085535 | Common:3; Rare:166 |