| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6739266-6739286 | Rare:5 | ||||
| chr19:6739495-6739779 | Common:6; Rare:85 | ||||
| chr19:6740809-6741044 | Rare:63 | ||||
| chr19:6761155-6761276 | Common:2; Rare:21 | ||||
| chr19:7069647-7069741 | Common:1; Rare:28 | ||||
| chr19:7395014-7395185 | Common:6; Rare:51 | ||||
| chr19:7488988-7489078 | Rare:42 | ||||
| chr19:7497448-7497610 | Common:3; Rare:30 | ||||
| chr19:7506875-7507110 | Common:2; Rare:61 | ||||
| chr19:7522518-7522685 | Rare:63; Clinvar:2 | ||||
| chr19:7535390-7535780 | Common:4; Rare:123; Clinvar:2 | ||||
| chr19:7629495-7629844 | Common:7; Rare:131; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7633589-7633831 | Common:2; Rare:38 | ||||
| chr19:7636969-7637161 | Common:2; Rare:59; Clinvar (benign):1 | ||||
| chr19:7641833-7642118 | Common:1; Rare:104; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 |