| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:33392370-33392840 | Common:5; Rare:157 | ||||
| chr19:33397110-33397510 | Common:6; Rare:160 | ||||
| chr19:33403350-33403940 | Common:8; Rare:190 | ||||
| chr19:34134417-34134616 | Common:6; Rare:131 | ||||
| chr19:34173369-34173532 | Common:4; Rare:52 | ||||
| chr19:34377251-34378020 | Common:12; Rare:272; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:34995640-34995853 | Rare:62 | ||||
| chr19:35575667-35575819 | Common:2; Rare:54 | ||||
| chr19:36127776-36128176 | Common:15; Rare:129 | ||||
| chr19:38700360-38701065 | Common:7; Rare:276; Clinvar (benign):2 | ||||
| chr19:38737510-38737900 | Common:7; Rare:220 | ||||
| chr19:38763487-38764245 | Common:11; Rare:220 | ||||
| chr19:38819146-38819647 | Common:4; Rare:160 | ||||
| chr19:38976423-38976707 | Common:2; Rare:65 | ||||
| chr19:39401481-39401860 | Common:1; Rare:145 |