| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:51108280-51108632 | Common:2; Rare:77 | ||||
| chr19:51108839-51108896 | Rare:14 | ||||
| chr19:51224993-51225148 | Common:1; Rare:41 | ||||
| chr19:51339719-51340054 | Common:1; Rare:75 | ||||
| chr19:51366229-51366649 | Common:8; Rare:131; Clinvar (benign):2 | ||||
| chr19:51367431-51367652 | Common:2; Rare:81 | ||||
| chr19:51367802-51368162 | Common:4; Rare:136 | ||||
| chr19:51417048-51417232 | Common:1; Rare:52 | ||||
| chr19:51417522-51417717 | Common:2; Rare:53 | ||||
| chr19:51417844-51417968 | Rare:14 | ||||
| chr19:51501791-51501858 | Rare:16 | ||||
| chr19:51531654-51531909 | Common:8; Rare:52 | ||||
| chr19:51571114-51571316 | Common:4; Rare:58 | ||||
| chr19:51904586-51904644 | Common:1; Rare:19 | ||||
| chr19:51904939-51905060 | Common:3; Rare:42 |