| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38769697-38770102 | Common:21; Rare:298 | ||||
| chr19:38831124-38831341 | Common:4; Rare:148 | ||||
| chr19:38831634-38832099 | Common:27; Rare:629; Clinvar (benign):6 | ||||
| chr19:38849209-38849666 | Common:5; Rare:564 | ||||
| chr19:38849610-38850956 | Common:17; Rare:1495 | ||||
| chr19:38851011-38851496 | Common:2; Rare:183 | ||||
| chr19:38851807-38852210 | Common:15; Rare:658 | ||||
| chr19:38852311-38852831 | Common:5; Rare:551 | ||||
| chr19:38877980-38878600 | Common:5; Rare:176 | ||||
| chr19:38899466-38900079 | Rare:989 | ||||
| chr19:38900193-38900300 | Common:1; Rare:44 | ||||
| chr19:38930294-38931069 | Common:25; Rare:1008; Clinvar:21; Clinvar (benign):26; Clinvar (pathogenic):3 | ||||
| chr19:38975234-38975508 | Common:1; Rare:45 | ||||
| chr19:38975422-38975531 | Rare:18 | ||||
| chr19:38975590-38976050 | Common:5; Rare:305 |