| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7561063-7561237 | Common:3; Rare:48; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:7629530-7629839 | Common:5; Rare:109; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636998-7637195 | Common:2; Rare:61; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:7642206-7642531 | Common:2; Rare:117; Clinvar:4; Clinvar (benign):4 | ||||
| chr19:7911151-7911324 | Common:6; Rare:99 | ||||
| chr19:7920225-7920369 | Rare:62 | ||||
| chr19:7943644-7943990 | Rare:90 | ||||
| chr19:8005498-8005821 | Common:1; Rare:113 | ||||
| chr19:8052475-8052792 | Common:2; Rare:54 | ||||
| chr19:8321308-8321702 | Common:2; Rare:159 | ||||
| chr19:8363532-8363782 | Common:4; Rare:61 | ||||
| chr19:8364012-8364167 | Common:1; Rare:41 | ||||
| chr19:8390056-8390453 | Common:2; Rare:111 | ||||
| chr19:8514133-8514232 | Common:1; Rare:30 | ||||
| chr19:8526424-8526490 | Rare:28; Clinvar (benign):1 |