| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39402578-39402978 | Rare:163 | ||||
| chr19:39411150-39411520 | Common:2; Rare:138 | ||||
| chr19:39453120-39453730 | Common:5; Rare:260 | ||||
| chr19:40190770-40191180 | Common:1; Rare:130 | ||||
| chr19:40433070-40433560 | Common:6; Rare:103 | ||||
| chr19:40433793-40434280 | Common:5; Rare:212 | ||||
| chr19:41176188-41176390 | Common:2; Rare:38 | ||||
| chr19:41352970-41353320 | Common:8; Rare:159; Clinvar (benign):4 | ||||
| chr19:41868651-41869320 | Common:7; Rare:284; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr19:42300150-42300470 | Common:1; Rare:84 | ||||
| chr19:42424873-42424994 | Rare:22 | ||||
| chr19:42443752-42444222 | Common:3; Rare:187 | ||||
| chr19:42488820-42489280 | Common:4; Rare:104 | ||||
| chr19:42497737-42498087 | Common:2; Rare:109 | ||||
| chr19:44571840-44572030 | Rare:25 |