| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46197992-46198112 | Common:9; Rare:20 | ||||
| chr19:46203078-46203228 | Common:2; Rare:20 | ||||
| chr19:46410555-46410805 | Common:1; Rare:48 | ||||
| chr19:46411080-46411303 | Common:1; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:46605802-46605855 | Rare:10; Clinvar (benign):1 | ||||
| chr19:46860773-46861135 | Common:3; Rare:115 | ||||
| chr19:46927233-46927471 | Rare:29 | ||||
| chr19:47350423-47350740 | Common:1; Rare:67 | ||||
| chr19:47719088-47719229 | Common:1; Rare:26 | ||||
| chr19:47744731-47744765 | Rare:4 | ||||
| chr19:48378632-48378822 | Common:1; Rare:36 | ||||
| chr19:48485732-48486037 | Rare:76 | ||||
| chr19:48707451-48707688 | Common:3; Rare:30 | ||||
| chr19:48924508-48924662 | Rare:27 | ||||
| chr19:48927017-48927276 | Common:2; Rare:41 |