| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:34926831-34926913 | Common:1; Rare:35 | ||||
| chr19:35269030-35269144 | Common:1; Rare:14 | ||||
| chr19:35545482-35545698 | Common:4; Rare:70 | ||||
| chr19:35612653-35612792 | Common:1; Rare:49 | ||||
| chr19:35628864-35629115 | Common:4; Rare:78 | ||||
| chr19:35648093-35648402 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:35740539-35740808 | Common:5; Rare:98 | ||||
| chr19:35745397-35745688 | Rare:87 | ||||
| chr19:35748286-35748600 | Common:3; Rare:89 | ||||
| chr19:35757883-35758201 | Common:2; Rare:95 | ||||
| chr19:35899745-35899865 | Common:1; Rare:37 | ||||
| chr19:35900515-35900749 | Common:1; Rare:56 | ||||
| chr19:36014192-36014551 | Common:2; Rare:97 | ||||
| chr19:36054223-36054462 | Common:1; Rare:73 | ||||
| chr19:36054753-36054944 | Common:1; Rare:61; Clinvar (benign):1 |