| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476209-50476547 | Common:1; Rare:160 | ||||
| chr19:50723174-50723377 | Common:2; Rare:49 | ||||
| chr19:50804592-50804906 | Common:6; Rare:94 | ||||
| chr19:51019702-51019989 | Common:5; Rare:53 | ||||
| chr19:51366322-51366551 | Common:5; Rare:65; Clinvar (benign):2 | ||||
| chr19:52008182-52008349 | Rare:46 | ||||
| chr19:52028325-52028462 | Common:3; Rare:33 | ||||
| chr19:52397750-52397890 | Common:4; Rare:43 | ||||
| chr19:52735030-52735148 | Common:2; Rare:31 | ||||
| chr19:53132869-53132927 | Common:2; Rare:18 | ||||
| chr19:53254814-53255019 | Common:1; Rare:69 | ||||
| chr19:53866348-53866397 | Common:1; Rare:11 | ||||
| chr19:54115289-54115415 | Common:1; Rare:26; Clinvar (benign):1 | ||||
| chr19:54115628-54115793 | Common:1; Rare:40; Clinvar:4 | ||||
| chr19:54159679-54160062 | Rare:134 |