| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11346738-11346786 | Rare:6 | ||||
| chr19:11355332-11355563 | Common:1; Rare:71 | ||||
| chr19:11374536-11374764 | Common:1; Rare:84 | ||||
| chr19:11374838-11375251 | Common:2; Rare:138 | ||||
| chr19:11381016-11381124 | Rare:35 | ||||
| chr19:11381147-11381468 | Common:2; Rare:106; Clinvar:1 | ||||
| chr19:11381607-11381620 | Rare:4 | ||||
| chr19:11381716-11381864 | Rare:56; Clinvar (benign):2 | ||||
| chr19:11435459-11435709 | Common:4; Rare:95; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:11435929-11436095 | Rare:44; Clinvar:1 | ||||
| chr19:11505248-11505431 | Rare:66 | ||||
| chr19:11505657-11506012 | Common:2; Rare:146 | ||||
| chr19:11529017-11529345 | Common:1; Rare:68 | ||||
| chr19:11559148-11559459 | Common:4; Rare:96 | ||||
| chr19:11597273-11597593 | Common:2; Rare:89 |