| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41309438-41309838 | Common:2; Rare:68 | ||||
| chr19:41310026-41310900 | Common:3; Rare:840 | ||||
| chr19:41350405-41351805 | Common:28; Rare:856 | ||||
| chr19:41353292-41354280 | Common:10; Rare:938 | ||||
| chr19:41363628-41364149 | Common:7; Rare:623; Clinvar:13 | ||||
| chr19:41364065-41364445 | Common:4; Rare:394; Clinvar:13 | ||||
| chr19:41397262-41397890 | Common:68; Rare:948; Clinvar (benign):29 | ||||
| chr19:41398016-41398416 | Common:3; Rare:71 | ||||
| chr19:41427030-41428394 | Common:21; Rare:1242 | ||||
| chr19:41439393-41439805 | Common:10; Rare:352 | ||||
| chr19:41439803-41440203 | Common:11; Rare:349 | ||||
| chr19:41549190-41549590 | Common:9; Rare:176 | ||||
| chr19:41843312-41843712 | Common:3; Rare:118 | ||||
| chr19:41859461-41860000 | Common:6; Rare:606; Clinvar:1 | ||||
| chr19:41859990-41860325 | Common:9; Rare:613; Clinvar:23; Clinvar (benign):12 |