| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42217697-42217877 | Rare:67 | ||||
| chr19:42220128-42220356 | Common:2; Rare:62 | ||||
| chr19:42302416-42302498 | Rare:19 | ||||
| chr19:42442904-42442932 | Rare:4 | ||||
| chr19:42528439-42528756 | Common:3; Rare:60 | ||||
| chr19:43465599-43465783 | Common:1; Rare:51 | ||||
| chr19:43527137-43527310 | Common:5; Rare:66; Clinvar:4; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575460-43575800 | Common:2; Rare:93 | ||||
| chr19:43901755-43901882 | Common:1; Rare:25 | ||||
| chr19:44002764-44002988 | Common:6; Rare:53 | ||||
| chr19:44071984-44072173 | Common:1; Rare:44 | ||||
| chr19:44141410-44141648 | Common:3; Rare:33 | ||||
| chr19:44305001-44305140 | Rare:36 | ||||
| chr19:44356645-44356851 | Common:1; Rare:43 | ||||
| chr19:44500205-44500295 | Common:2; Rare:47 |