| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48473905-48474281 | Common:3; Rare:116 | ||||
| chr19:48478310-48478626 | Common:1; Rare:121 | ||||
| chr19:48600372-48600629 | Common:4; Rare:50 | ||||
| chr19:48714029-48714399 | Common:3; Rare:98 | ||||
| chr19:48714592-48714662 | Rare:16 | ||||
| chr19:48811991-48812132 | Rare:23 | ||||
| chr19:48820873-48821003 | Common:1; Rare:27 | ||||
| chr19:48821994-48822277 | Common:1; Rare:68 | ||||
| chr19:48875486-48875548 | Rare:11 | ||||
| chr19:48902445-48902598 | Rare:17 | ||||
| chr19:48966329-48966728 | Rare:129; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr19:48988414-48988478 | Rare:12 | ||||
| chr19:48990506-48990559 | Common:1; Rare:13 | ||||
| chr19:48990729-48991011 | Common:1; Rare:47 | ||||
| chr19:49009802-49010057 | Common:1; Rare:98 |