| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39390719-39390735 | Rare:3 | ||||
| chr19:39390816-39390948 | Rare:50; Clinvar:1 | ||||
| chr19:39390962-39391477 | Common:1; Rare:196 | ||||
| chr19:39406710-39406860 | Rare:57 | ||||
| chr19:39412335-39412626 | Common:2; Rare:113 | ||||
| chr19:39435569-39436133 | Common:6; Rare:224 | ||||
| chr19:39445434-39446127 | Common:4; Rare:200 | ||||
| chr19:39468824-39469095 | Common:1; Rare:54 | ||||
| chr19:39471385-39471620 | Rare:54 | ||||
| chr19:39480795-39480964 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
| chr19:39481679-39482033 | Rare:98 | ||||
| chr19:39834053-39834558 | Common:3; Rare:146 | ||||
| chr19:39840242-39840515 | Common:1; Rare:81 | ||||
| chr19:39846159-39846499 | Common:1; Rare:139 | ||||
| chr19:39970948-39971246 | Common:3; Rare:82 |