| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39480716-39480931 | Common:3; Rare:114; Clinvar (pathogenic):1 | ||||
| chr19:39737988-39738167 | Common:2; Rare:25 | ||||
| chr19:39846296-39846477 | Common:1; Rare:84 | ||||
| chr19:39970918-39971221 | Common:4; Rare:86 | ||||
| chr19:39996944-39997119 | Common:5; Rare:58 | ||||
| chr19:40056137-40056246 | Rare:15 | ||||
| chr19:40090878-40090968 | Common:1; Rare:24 | ||||
| chr19:40280830-40280935 | Rare:21 | ||||
| chr19:40285186-40285456 | Common:1; Rare:88 | ||||
| chr19:40348388-40348740 | Common:4; Rare:118 | ||||
| chr19:40444263-40444517 | Common:3; Rare:79 | ||||
| chr19:40465568-40466112 | Common:3; Rare:194 | ||||
| chr19:40715074-40715148 | Rare:24 | ||||
| chr19:40716848-40716953 | Rare:32 | ||||
| chr19:40750386-40750560 | Common:3; Rare:55 |