| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390845-39390957 | Rare:41 | ||||
| chr19:39390974-39391461 | Common:1; Rare:187 | ||||
| chr19:39406656-39406873 | Rare:72 | ||||
| chr19:39435854-39436154 | Common:6; Rare:107 | ||||
| chr19:39445459-39445773 | Common:2; Rare:90 | ||||
| chr19:39480628-39480958 | Common:3; Rare:158; Clinvar (pathogenic):1 | ||||
| chr19:39846308-39846479 | Common:1; Rare:82 | ||||
| chr19:39970957-39971223 | Common:3; Rare:73 | ||||
| chr19:39996925-39997118 | Common:5; Rare:62 | ||||
| chr19:40056137-40056268 | Rare:17 | ||||
| chr19:40090858-40091006 | Common:1; Rare:40 | ||||
| chr19:40285189-40285637 | Common:4; Rare:148 | ||||
| chr19:40348347-40348760 | Common:4; Rare:132 | ||||
| chr19:40366389-40366920 | Rare:160 | ||||
| chr19:40369990-40370237 | Rare:82 |