| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49665826-49666020 | Common:2; Rare:99; Clinvar (pathogenic):1 | ||||
| chr19:49867539-49867666 | Common:2; Rare:38 | ||||
| chr19:51366333-51366677 | Common:8; Rare:92; Clinvar (benign):2 | ||||
| chr19:52397733-52397879 | Common:2; Rare:43 | ||||
| chr19:53869324-53869707 | Common:3; Rare:99 | ||||
| chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
| chr19:54200728-54200893 | Common:3; Rare:64 | ||||
| chr19:54449032-54449247 | Common:2; Rare:64 | ||||
| chr19:55385751-55385982 | Common:6; Rare:79 | ||||
| chr19:55654893-55655087 | Rare:76 | ||||
| chr19:56393517-56393675 | Common:2; Rare:50 | ||||
| chr19:57280325-57280493 | Common:1; Rare:54 | ||||
| chr19:57435150-57435339 | Common:6; Rare:34 | ||||
| chr19:57889026-57889215 | Rare:54 | ||||
| chr19:58278801-58278991 | Common:1; Rare:55 |