| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41352453-41352853 | Common:2; Rare:153 | ||||
| chr19:41352870-41353280 | Common:5; Rare:107; Clinvar (benign):3 | ||||
| chr19:41940260-41940580 | Rare:76 | ||||
| chr19:41995996-41996305 | Common:1; Rare:62 | ||||
| chr19:42150976-42151376 | Common:4; Rare:128 | ||||
| chr19:42244704-42244947 | Rare:64 | ||||
| chr19:42282377-42283092 | Common:3; Rare:176 | ||||
| chr19:42387009-42387465 | Common:2; Rare:286 | ||||
| chr19:42396854-42397201 | Common:1; Rare:85 | ||||
| chr19:42401390-42401830 | Common:4; Rare:105 | ||||
| chr19:42401850-42402260 | Common:5; Rare:122; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr19:43475278-43475502 | Common:2; Rare:109 | ||||
| chr19:43635070-43635600 | Rare:102 | ||||
| chr19:43687240-43687700 | Common:7; Rare:60 | ||||
| chr19:43699640-43699940 | Rare:53 |