| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45584700-45585101 | Common:5; Rare:144; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:45639312-45639494 | Common:1; Rare:57 | ||||
| chr19:45641423-45641887 | Common:2; Rare:115 | ||||
| chr19:45642137-45642481 | Common:2; Rare:116 | ||||
| chr19:45642486-45642682 | Rare:33 | ||||
| chr19:45645577-45645802 | Common:3; Rare:46 | ||||
| chr19:45645925-45646009 | Common:1; Rare:12 | ||||
| chr19:45668067-45668250 | Common:2; Rare:37 | ||||
| chr19:45677362-45677640 | Common:2; Rare:55 | ||||
| chr19:45691852-45692044 | Rare:75 | ||||
| chr19:45692488-45692798 | Common:3; Rare:92 | ||||
| chr19:45730824-45731162 | Common:1; Rare:75 | ||||
| chr19:45768228-45768629 | Rare:156; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:45769195-45769712 | Common:3; Rare:212 | ||||
| chr19:45792133-45792379 | Rare:59 |