| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48543317-48543717 | Common:3; Rare:196 | ||||
| chr19:48553780-48554100 | Common:4; Rare:73 | ||||
| chr19:48554402-48554802 | Common:3; Rare:54 | ||||
| chr19:48568350-48568870 | Common:8; Rare:106 | ||||
| chr19:48569956-48570150 | Common:1; Rare:37 | ||||
| chr19:48574700-48575010 | Common:3; Rare:59 | ||||
| chr19:48635900-48636255 | Rare:124 | ||||
| chr19:48668860-48669260 | Common:11; Rare:80 | ||||
| chr19:48713974-48714687 | Common:12; Rare:468 | ||||
| chr19:48720300-48721018 | Common:7; Rare:321 | ||||
| chr19:48812210-48812630 | Common:18; Rare:234 | ||||
| chr19:48819520-48819850 | Rare:45 | ||||
| chr19:48872930-48873330 | Common:10; Rare:140 | ||||
| chr19:48956626-48957260 | Common:8; Rare:141 | ||||
| chr19:48965833-48966413 | Common:6; Rare:361; Clinvar:4; Clinvar (pathogenic):5 |