| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41351384-41351805 | Common:4; Rare:76 | ||||
| chr19:41353570-41353733 | Rare:40 | ||||
| chr19:41353828-41354134 | Common:1; Rare:95 | ||||
| chr19:41363726-41364077 | Common:1; Rare:107; Clinvar:2 | ||||
| chr19:41364123-41364434 | Rare:98; Clinvar:1 | ||||
| chr19:41397256-41397413 | Common:3; Rare:64 | ||||
| chr19:41397517-41397891 | Common:8; Rare:127; Clinvar (benign):7 | ||||
| chr19:41439525-41439722 | Common:2; Rare:54 | ||||
| chr19:41439818-41440076 | Common:3; Rare:106 | ||||
| chr19:41549221-41549251 | Rare:3 | ||||
| chr19:41549253-41549535 | Common:3; Rare:57 | ||||
| chr19:41576032-41576246 | Common:2; Rare:38 | ||||
| chr19:41859520-41859937 | Common:1; Rare:115 | ||||
| chr19:41860001-41860350 | Common:3; Rare:128; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:41877003-41877348 | Common:1; Rare:70; Clinvar:1; Clinvar (benign):1 |