| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38975685-38975854 | Common:1; Rare:44 | ||||
| chr19:39390981-39391425 | Common:1; Rare:170 | ||||
| chr19:39406701-39406887 | Rare:75 | ||||
| chr19:39412282-39412792 | Common:3; Rare:189 | ||||
| chr19:39412822-39412888 | Rare:10 | ||||
| chr19:39435781-39436182 | Common:7; Rare:159 | ||||
| chr19:39445470-39445756 | Common:2; Rare:82 | ||||
| chr19:39480602-39480961 | Common:3; Rare:167; Clinvar (pathogenic):1 | ||||
| chr19:39846302-39846473 | Common:1; Rare:81 | ||||
| chr19:39970859-39971215 | Common:5; Rare:100 | ||||
| chr19:39996925-39997101 | Common:5; Rare:56 | ||||
| chr19:40056154-40056277 | Rare:18 | ||||
| chr19:40090871-40091029 | Common:1; Rare:43 | ||||
| chr19:40285243-40285537 | Common:1; Rare:108 | ||||
| chr19:40348388-40348724 | Common:4; Rare:110 |