| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10517416-10517555 | Common:1; Rare:32 | ||||
| chr19:10565966-10566214 | Common:2; Rare:84 | ||||
| chr19:10568965-10569221 | Common:2; Rare:67 | ||||
| chr19:10631629-10631947 | Common:2; Rare:109 | ||||
| chr19:10653817-10654132 | Common:1; Rare:120 | ||||
| chr19:10795941-10796197 | Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:10798398-10798566 | Rare:52; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:10836277-10836570 | Common:2; Rare:77 | ||||
| chr19:10928557-10928726 | Common:1; Rare:45 | ||||
| chr19:10960689-10961164 | Common:3; Rare:173; Clinvar (benign):2 | ||||
| chr19:11197504-11197637 | Common:1; Rare:40 | ||||
| chr19:11374889-11375245 | Common:1; Rare:113 | ||||
| chr19:11384239-11384376 | Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:11419280-11419440 | Common:1; Rare:33 | ||||
| chr19:11435180-11435440 | Common:2; Rare:68 |