| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965357-48965609 | Rare:80; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993253-48993586 | Common:3; Rare:145; Clinvar:3; Clinvar (benign):2 | ||||
| chr19:49085123-49085515 | Common:3; Rare:162 | ||||
| chr19:49149258-49149501 | Rare:80 | ||||
| chr19:49149646-49149961 | Common:1; Rare:67 | ||||
| chr19:49335404-49335478 | Common:1; Rare:18 | ||||
| chr19:49362374-49362520 | Rare:42 | ||||
| chr19:49451735-49451996 | Common:3; Rare:67 | ||||
| chr19:49496322-49496470 | Common:1; Rare:61 | ||||
| chr19:49513087-49513417 | Common:1; Rare:74 | ||||
| chr19:49580528-49580650 | Rare:42 | ||||
| chr19:49665718-49665989 | Common:3; Rare:119; Clinvar (pathogenic):1 | ||||
| chr19:49690980-49691150 | Common:2; Rare:39 | ||||
| chr19:49818239-49818338 | Common:3; Rare:51; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49851001-49851026 | Rare:11 |