| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51366335-51366545 | Common:5; Rare:55; Clinvar (benign):2 | ||||
| chr19:52028372-52028471 | Common:2; Rare:17 | ||||
| chr19:52397750-52397879 | Common:2; Rare:38 | ||||
| chr19:53333560-53333768 | Common:3; Rare:66 | ||||
| chr19:54115638-54115797 | Common:1; Rare:36; Clinvar:4 | ||||
| chr19:54189305-54189408 | Common:1; Rare:29 | ||||
| chr19:54200728-54200870 | Common:2; Rare:52 | ||||
| chr19:54449049-54449222 | Common:2; Rare:48 | ||||
| chr19:55385738-55385976 | Common:6; Rare:80 | ||||
| chr19:55654851-55655053 | Rare:68 | ||||
| chr19:58228817-58228955 | Common:2; Rare:56 | ||||
| chr19:58278734-58278981 | Common:2; Rare:77 | ||||
| chr19:58326872-58327019 | Common:1; Rare:30 | ||||
| chr19:58408495-58408678 | Common:1; Rare:57 | ||||
| chr2:677364-677628 | Common:2; Rare:101 |