| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17306055-17306142 | Rare:21 | ||||
| chr19:17306330-17306357 | Rare:9 | ||||
| chr19:17309245-17309625 | Common:3; Rare:108 | ||||
| chr19:17310335-17310549 | Common:1; Rare:35 | ||||
| chr19:17334411-17334577 | Common:1; Rare:37 | ||||
| chr19:17334730-17334909 | Common:2; Rare:69 | ||||
| chr19:17336611-17336796 | Rare:38 | ||||
| chr19:17337088-17337159 | Rare:15 | ||||
| chr19:17337286-17337672 | Common:1; Rare:95; Clinvar:1 | ||||
| chr19:17338037-17338204 | Common:1; Rare:64; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:17405333-17405888 | Common:7; Rare:140 | ||||
| chr19:17419720-17420142 | Common:18; Rare:122 | ||||
| chr19:17448652-17448791 | Rare:38 | ||||
| chr19:17469664-17470076 | Common:2; Rare:78 | ||||
| chr19:17470126-17470538 | Common:2; Rare:123 |