| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45885862-45885971 | Rare:21 | ||||
| chr19:45886051-45886303 | Common:4; Rare:92 | ||||
| chr19:45886454-45886661 | Common:5; Rare:37 | ||||
| chr19:45902523-45902952 | Common:4; Rare:128 | ||||
| chr19:45994992-45995438 | Common:3; Rare:178 | ||||
| chr19:46346856-46347146 | Common:3; Rare:101 | ||||
| chr19:46347361-46347570 | Rare:43 | ||||
| chr19:46600509-46600704 | Rare:42 | ||||
| chr19:46600913-46601411 | Common:5; Rare:172; Clinvar (benign):1 | ||||
| chr19:46625063-46625422 | Common:1; Rare:62 | ||||
| chr19:46713771-46714040 | Common:1; Rare:81 | ||||
| chr19:46714059-46714371 | Common:1; Rare:62 | ||||
| chr19:46714525-46714782 | Common:2; Rare:57 | ||||
| chr19:46716837-46716866 | Rare:3 | ||||
| chr19:46716902-46717526 | Common:5; Rare:147 |