| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10194948-10195158 | Common:1; Rare:80; Clinvar (benign):1 | ||||
| chr19:10230870-10231510 | Common:5; Rare:153 | ||||
| chr19:10251747-10251987 | Common:2; Rare:55 | ||||
| chr19:10252060-10252280 | Common:2; Rare:83 | ||||
| chr19:10315940-10316089 | Common:3; Rare:80; Clinvar (benign):7 | ||||
| chr19:10332877-10333323 | Rare:113 | ||||
| chr19:10333500-10333754 | Rare:81 | ||||
| chr19:10380422-10380881 | Common:13; Rare:141; Clinvar:5 | ||||
| chr19:10403480-10403692 | Rare:106 | ||||
| chr19:10419989-10420568 | Common:3; Rare:237 | ||||
| chr19:10502674-10503006 | Rare:92 | ||||
| chr19:10503246-10503865 | Common:13; Rare:247 | ||||
| chr19:10516722-10517447 | Common:8; Rare:193 | ||||
| chr19:10543720-10543953 | Common:1; Rare:67 | ||||
| chr19:10565982-10566116 | Common:2; Rare:52 |