| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:42316900-42317032 | Rare:44 | ||||
| chr19:42387109-42387235 | Rare:36 | ||||
| chr19:42396324-42396611 | Rare:46 | ||||
| chr19:42396799-42397241 | Common:1; Rare:104 | ||||
| chr19:42401921-42401969 | Rare:20; Clinvar (pathogenic):1 | ||||
| chr19:42450491-42450535 | Rare:8 | ||||
| chr19:42465878-42466080 | Common:1; Rare:42 | ||||
| chr19:42466685-42466854 | Rare:20 | ||||
| chr19:43475277-43475500 | Common:2; Rare:109 | ||||
| chr19:43503605-43503791 | Common:1; Rare:26 | ||||
| chr19:43562705-43562814 | Rare:19 | ||||
| chr19:43594825-43594920 | Rare:33 | ||||
| chr19:43675389-43675513 | Rare:18 | ||||
| chr19:43752009-43752152 | Common:1; Rare:28 | ||||
| chr19:43756829-43756908 | Rare:18 |