| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48672959-48673345 | Rare:111 | ||||
| chr19:48810872-48811126 | Rare:82 | ||||
| chr19:48868557-48868691 | Rare:29 | ||||
| chr19:48872210-48872421 | Common:2; Rare:61 | ||||
| chr19:48900157-48900394 | Common:1; Rare:78 | ||||
| chr19:48954647-48954925 | Common:1; Rare:100 | ||||
| chr19:48993287-48993547 | Common:3; Rare:112; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:49085103-49085531 | Common:3; Rare:170 | ||||
| chr19:49128433-49128609 | Common:1; Rare:51 | ||||
| chr19:49487284-49487644 | Common:5; Rare:129 | ||||
| chr19:49513116-49513405 | Common:1; Rare:68 | ||||
| chr19:49580536-49580733 | Common:1; Rare:55 | ||||
| chr19:49665756-49666038 | Common:3; Rare:135; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691138 | Rare:36 | ||||
| chr19:49813171-49813350 | Rare:72 |