| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:43901607-43901916 | Common:3; Rare:61 | ||||
| chr19:44002784-44003006 | Common:4; Rare:61 | ||||
| chr19:44072047-44072193 | Common:2; Rare:37 | ||||
| chr19:44113120-44113498 | Common:5; Rare:81 | ||||
| chr19:44304974-44305171 | Rare:60 | ||||
| chr19:44356652-44356851 | Common:1; Rare:41 | ||||
| chr19:44643788-44643997 | Rare:58 | ||||
| chr19:44757362-44757569 | Rare:52; Clinvar:1 | ||||
| chr19:45092824-45093228 | Common:3; Rare:119 | ||||
| chr19:45406359-45406694 | Common:3; Rare:84 | ||||
| chr19:45496996-45497259 | Common:2; Rare:87 | ||||
| chr19:45584763-45585054 | Common:4; Rare:111; Clinvar:2; Clinvar (benign):4 | ||||
| chr19:45692331-45692722 | Common:1; Rare:92 | ||||
| chr19:45768231-45768355 | Rare:52; Clinvar (benign):1 | ||||
| chr19:46600913-46601416 | Common:5; Rare:173; Clinvar (benign):1 |