| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48811012-48811085 | Rare:30 | ||||
| chr19:48872218-48872427 | Common:2; Rare:64 | ||||
| chr19:48900188-48900367 | Common:1; Rare:61 | ||||
| chr19:48965689-48965802 | Rare:38 | ||||
| chr19:48993259-48993575 | Common:3; Rare:139; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:48993775-48993913 | Common:3; Rare:45 | ||||
| chr19:49361515-49361731 | Rare:38 | ||||
| chr19:49362367-49362487 | Rare:34 | ||||
| chr19:49513072-49513398 | Common:1; Rare:70 | ||||
| chr19:49527837-49528011 | Common:3; Rare:55 | ||||
| chr19:49580528-49580645 | Rare:42 | ||||
| chr19:49665756-49666029 | Common:3; Rare:134; Clinvar (pathogenic):1 | ||||
| chr19:49813245-49813341 | Rare:39 | ||||
| chr19:49867553-49867646 | Common:2; Rare:28 | ||||
| chr19:49877299-49877724 | Common:1; Rare:111 |