| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192540-19192996 | Common:5; Rare:237; Clinvar (benign):1 | ||||
| chr19:19203246-19203563 | Common:2; Rare:167 | ||||
| chr19:19320471-19321054 | Common:11; Rare:370 | ||||
| chr19:19385451-19385874 | Rare:107 | ||||
| chr19:19385877-19386049 | Rare:115 | ||||
| chr19:19405502-19405855 | Common:8; Rare:229 | ||||
| chr19:19516106-19516300 | Rare:220; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr19:19618651-19618918 | Rare:85 | ||||
| chr19:19643549-19643738 | Common:6; Rare:109 | ||||
| chr19:19663461-19663759 | Rare:99 | ||||
| chr19:19663940-19664230 | Common:3; Rare:110 | ||||
| chr19:19668651-19668883 | Common:2; Rare:68 | ||||
| chr19:19733073-19733224 | Common:2; Rare:62 | ||||
| chr19:21082021-21082323 | Common:1; Rare:105 | ||||
| chr19:23395376-23395656 | Common:1; Rare:139 |