| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49085096-49085492 | Common:3; Rare:154 | ||||
| chr19:49114227-49114416 | Common:4; Rare:50 | ||||
| chr19:49119093-49119386 | Rare:90 | ||||
| chr19:49149332-49149528 | Common:1; Rare:72 | ||||
| chr19:49149622-49149986 | Common:1; Rare:80 | ||||
| chr19:49157644-49157827 | Rare:52; Clinvar:1 | ||||
| chr19:49335279-49335406 | Rare:20 | ||||
| chr19:49362380-49362502 | Rare:38 | ||||
| chr19:49423634-49423801 | Rare:27 | ||||
| chr19:49451735-49452015 | Common:3; Rare:78 | ||||
| chr19:49453024-49453300 | Common:2; Rare:84 | ||||
| chr19:49489768-49489967 | Common:1; Rare:75 | ||||
| chr19:49513108-49513276 | Common:1; Rare:37 | ||||
| chr19:49580527-49580650 | Rare:43 | ||||
| chr19:49665777-49665989 | Common:2; Rare:104; Clinvar (pathogenic):1 |