| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777892-40778298 | Common:1; Rare:109 | ||||
| chr19:41262267-41262644 | Rare:61 | ||||
| chr19:41310047-41310309 | Rare:100 | ||||
| chr19:41310447-41310483 | Rare:9 | ||||
| chr19:41353920-41354070 | Rare:55 | ||||
| chr19:41364084-41364154 | Common:1; Rare:21; Clinvar:2 | ||||
| chr19:41397558-41397853 | Common:7; Rare:104; Clinvar (benign):5 | ||||
| chr19:41549278-41549520 | Common:3; Rare:47 | ||||
| chr19:41860099-41860466 | Common:5; Rare:148; Clinvar:4; Clinvar (benign):2 | ||||
| chr19:41876982-41877171 | Rare:32 | ||||
| chr19:41877204-41877383 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:41882915-41883281 | Common:1; Rare:69 | ||||
| chr19:41884132-41884446 | Rare:77 | ||||
| chr19:41904036-41904301 | Common:1; Rare:81 | ||||
| chr19:41905760-41906047 | Common:1; Rare:89 |