| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41860977-41861209 | Rare:75; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41892352-41892676 | Common:2; Rare:86 | ||||
| chr19:42075817-42076191 | Rare:102 | ||||
| chr19:42132436-42132627 | Rare:37 | ||||
| chr19:42217764-42218047 | Common:2; Rare:83 | ||||
| chr19:42220112-42220333 | Common:2; Rare:61 | ||||
| chr19:42268432-42268557 | Rare:26 | ||||
| chr19:42283781-42284085 | Rare:105 | ||||
| chr19:42412389-42412571 | Common:1; Rare:37 | ||||
| chr19:42423543-42423790 | Common:4; Rare:81 | ||||
| chr19:43527169-43527314 | Common:5; Rare:56; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr19:43575495-43575807 | Common:2; Rare:81 | ||||
| chr19:43596045-43596425 | Common:3; Rare:118 | ||||
| chr19:43670140-43670306 | Common:2; Rare:37 | ||||
| chr19:43754901-43755102 | Common:3; Rare:69 |