| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46298120-46298473 | Common:5; Rare:85 | ||||
| chr19:46600968-46601347 | Common:4; Rare:129 | ||||
| chr19:46745847-46746068 | Common:3; Rare:45 | ||||
| chr19:47256472-47256568 | Rare:33 | ||||
| chr19:47484261-47484298 | Rare:10 | ||||
| chr19:47745416-47745560 | Rare:66 | ||||
| chr19:48170259-48170696 | Common:2; Rare:119 | ||||
| chr19:48255552-48255729 | Common:1; Rare:28 | ||||
| chr19:48325437-48325609 | Common:2; Rare:41 | ||||
| chr19:48445909-48446053 | Common:1; Rare:60 | ||||
| chr19:48619145-48619428 | Rare:90 | ||||
| chr19:48810997-48811136 | Rare:47 | ||||
| chr19:48965368-48965609 | Rare:76; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993296-48993533 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:48993553-48993851 | Common:3; Rare:68 |