| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10090962-10091187 | Common:1; Rare:47 | ||||
| chr19:10251758-10252018 | Common:1; Rare:66 | ||||
| chr19:10270850-10271145 | Rare:75 | ||||
| chr19:10286720-10287125 | Common:2; Rare:102 | ||||
| chr19:10333484-10333734 | Common:1; Rare:87 | ||||
| chr19:10380487-10380792 | Common:11; Rare:89; Clinvar:5 | ||||
| chr19:10503304-10503613 | Common:2; Rare:61 | ||||
| chr19:10568965-10569230 | Common:2; Rare:68 | ||||
| chr19:10654151-10654393 | Common:4; Rare:118 | ||||
| chr19:10836274-10836575 | Common:3; Rare:77 | ||||
| chr19:10928541-10928699 | Common:1; Rare:40 | ||||
| chr19:10960689-10961077 | Common:3; Rare:154 | ||||
| chr19:11089347-11089551 | Rare:45; Clinvar:9; Clinvar (pathogenic):1 | ||||
| chr19:11197501-11197684 | Common:1; Rare:59 | ||||
| chr19:11197775-11197979 | Common:2; Rare:60 |