| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48390893-48390962 | Rare:6 | ||||
| chr19:48445914-48446191 | Common:1; Rare:113 | ||||
| chr19:48552108-48552315 | Rare:70 | ||||
| chr19:48619139-48619435 | Rare:96 | ||||
| chr19:48695747-48696023 | Common:2; Rare:61 | ||||
| chr19:48810988-48811085 | Rare:39 | ||||
| chr19:48964971-48965609 | Common:1; Rare:172; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
| chr19:48993196-48993510 | Common:3; Rare:138; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:49085144-49085634 | Common:3; Rare:194 | ||||
| chr19:49114171-49114429 | Common:4; Rare:67 | ||||
| chr19:49119112-49119374 | Rare:85 | ||||
| chr19:49128075-49128248 | Common:2; Rare:55 | ||||
| chr19:49147974-49148172 | Rare:35 | ||||
| chr19:49157580-49157869 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:49451649-49451852 | Common:1; Rare:42 |