| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:32345436-32345966 | Common:3; Rare:153 | ||||
| chr19:32346023-32346102 | Rare:28 | ||||
| chr19:32405121-32405132 | Rare:4 | ||||
| chr19:32405145-32405188 | Common:1; Rare:8 | ||||
| chr19:32405227-32405303 | Rare:24 | ||||
| chr19:32405385-32405814 | Common:4; Rare:163 | ||||
| chr19:32405887-32406175 | Common:2; Rare:89 | ||||
| chr19:32406181-32406281 | Rare:25 | ||||
| chr19:32580966-32581301 | Common:5; Rare:123 | ||||
| chr19:32581416-32581521 | Rare:35 | ||||
| chr19:32674743-32674841 | Rare:21 | ||||
| chr19:32674873-32675102 | Common:2; Rare:61 | ||||
| chr19:32675107-32675536 | Common:5; Rare:138 | ||||
| chr19:32676246-32676405 | Common:1; Rare:56; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:32691654-32691963 | Common:6; Rare:93 |