| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48872946-48873170 | Common:4; Rare:31 | ||||
| chr19:48873388-48873462 | Common:1; Rare:23 | ||||
| chr19:48875251-48875477 | Common:4; Rare:46 | ||||
| chr19:48927023-48927217 | Common:2; Rare:32 | ||||
| chr19:48963882-48964037 | Common:1; Rare:28 | ||||
| chr19:48964329-48964476 | Rare:28 | ||||
| chr19:48966203-48966301 | Rare:30; Clinvar:1 | ||||
| chr19:48969855-48970161 | Common:2; Rare:105; Clinvar (benign):1 | ||||
| chr19:48992297-48992445 | Rare:19 | ||||
| chr19:49151558-49151818 | Common:1; Rare:79 | ||||
| chr19:49176955-49177118 | Common:2; Rare:30 | ||||
| chr19:49196655-49196730 | Rare:21; Clinvar:1 | ||||
| chr19:49211490-49211694 | Rare:43; Clinvar:4 | ||||
| chr19:49211936-49212251 | Rare:60 | ||||
| chr19:49226124-49226293 | Common:3; Rare:40 |