| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6739435-6739780 | Common:12; Rare:181 | ||||
| chr19:6740498-6741131 | Common:1; Rare:204 | ||||
| chr19:6767201-6767978 | Common:9; Rare:155 | ||||
| chr19:7069091-7069470 | Common:2; Rare:149 | ||||
| chr19:7069663-7069961 | Common:3; Rare:106 | ||||
| chr19:7294302-7294628 | Common:8; Rare:123 | ||||
| chr19:7395015-7395265 | Common:10; Rare:126 | ||||
| chr19:7488959-7489147 | Common:2; Rare:129 | ||||
| chr19:7515800-7516280 | Common:2; Rare:158 | ||||
| chr19:7522296-7522686 | Common:2; Rare:112; Clinvar:2 | ||||
| chr19:7533854-7534218 | Common:6; Rare:142; Clinvar (benign):2 | ||||
| chr19:7535351-7535778 | Common:7; Rare:196; Clinvar:2 | ||||
| chr19:7595756-7595907 | Common:2; Rare:51 | ||||
| chr19:7629511-7629854 | Common:10; Rare:242; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr19:7636984-7637184 | Common:4; Rare:105; Clinvar (benign):2 |