| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48619139-48619573 | Common:1; Rare:145 | ||||
| chr19:48624042-48624414 | Common:1; Rare:90 | ||||
| chr19:48637708-48637791 | Rare:19 | ||||
| chr19:48811005-48811127 | Rare:42 | ||||
| chr19:48872247-48872427 | Common:2; Rare:60 | ||||
| chr19:48933584-48933702 | Common:3; Rare:34 | ||||
| chr19:48954724-48954916 | Rare:69 | ||||
| chr19:48965468-48965480 | Rare:3 | ||||
| chr19:48993265-48993579 | Common:3; Rare:137; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085103-49085515 | Common:3; Rare:167 | ||||
| chr19:49115041-49115177 | Rare:31 | ||||
| chr19:49119087-49119374 | Rare:91 | ||||
| chr19:49157660-49157835 | Rare:52; Clinvar:1 | ||||
| chr19:49335131-49335406 | Rare:45 | ||||
| chr19:49362380-49362497 | Rare:35 |