| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49098422-49098716 | Rare:73 | ||||
| chr19:49103830-49104594 | Common:1; Rare:228 | ||||
| chr19:49460832-49460960 | Common:1; Rare:33 | ||||
| chr19:49492233-49492388 | Common:3; Rare:52 | ||||
| chr19:49518694-49518842 | Common:1; Rare:32 | ||||
| chr19:49521595-49521813 | Common:1; Rare:34 | ||||
| chr19:49555811-49555956 | Common:2; Rare:53 | ||||
| chr19:49593398-49593698 | Common:1; Rare:111 | ||||
| chr19:49614199-49614423 | Rare:46 | ||||
| chr19:49614979-49615235 | Common:3; Rare:60 | ||||
| chr19:49635383-49635877 | Common:2; Rare:149; Clinvar:4; Clinvar (benign):5 | ||||
| chr19:49638005-49638252 | Common:1; Rare:65 | ||||
| chr19:49706772-49707044 | Rare:44 | ||||
| chr19:49719437-49719695 | Common:1; Rare:60 | ||||
| chr19:49818971-49819188 | Common:2; Rare:48 |