| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7636905-7637204 | Common:10; Rare:220; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:7680687-7680927 | Common:5; Rare:156 | ||||
| chr19:7681268-7682559 | Common:4; Rare:346 | ||||
| chr19:7874192-7875029 | Common:11; Rare:462 | ||||
| chr19:7888370-7888584 | Common:3; Rare:139 | ||||
| chr19:7894920-7895185 | Common:4; Rare:96 | ||||
| chr19:7903418-7903972 | Common:6; Rare:483 | ||||
| chr19:7916202-7917211 | Common:7; Rare:719 | ||||
| chr19:7920131-7920432 | Rare:257 | ||||
| chr19:7920757-7921126 | Rare:82 | ||||
| chr19:7925418-7926360 | Common:10; Rare:606 | ||||
| chr19:7928028-7929180 | Common:12; Rare:414; Clinvar (benign):2 | ||||
| chr19:7943568-7944064 | Common:1; Rare:364; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:8005534-8005889 | Common:3; Rare:337 | ||||
| chr19:8006011-8006411 | Common:5; Rare:120 |