| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48933590-48933702 | Common:3; Rare:33 | ||||
| chr19:48954724-48954960 | Rare:84 | ||||
| chr19:48965236-48965609 | Rare:115; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993277-48993914 | Common:8; Rare:217; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:49085088-49085541 | Common:3; Rare:177 | ||||
| chr19:49114203-49114406 | Common:4; Rare:52 | ||||
| chr19:49128029-49128261 | Common:2; Rare:70 | ||||
| chr19:49362375-49362474 | Rare:28 | ||||
| chr19:49451748-49452002 | Common:3; Rare:66 | ||||
| chr19:49453024-49453321 | Common:2; Rare:89 | ||||
| chr19:49453464-49453639 | Common:1; Rare:54 | ||||
| chr19:49487278-49487675 | Common:5; Rare:151 | ||||
| chr19:49489749-49489967 | Common:1; Rare:79 | ||||
| chr19:49496064-49496470 | Common:2; Rare:140 | ||||
| chr19:49580528-49580686 | Rare:51 |