| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41263030-41263162 | Common:2; Rare:25 | ||||
| chr19:41263641-41264018 | Rare:84 | ||||
| chr19:41264223-41264707 | Common:4; Rare:168 | ||||
| chr19:41264731-41264808 | Rare:24 | ||||
| chr19:41264872-41265126 | Common:2; Rare:51 | ||||
| chr19:41265198-41265345 | Rare:30 | ||||
| chr19:41310068-41310530 | Rare:157 | ||||
| chr19:41353870-41353957 | Rare:30 | ||||
| chr19:41363744-41364031 | Common:1; Rare:95; Clinvar:1 | ||||
| chr19:41364035-41364395 | Common:1; Rare:110; Clinvar:4 | ||||
| chr19:41376628-41376757 | Common:1; Rare:46 | ||||
| chr19:41397143-41397179 | Rare:7 | ||||
| chr19:41397279-41397500 | Common:4; Rare:66 | ||||
| chr19:41397573-41397855 | Common:7; Rare:100; Clinvar (benign):5 | ||||
| chr19:41427303-41427571 | Rare:78 |