| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49877264-49877717 | Common:2; Rare:111 | ||||
| chr19:49929119-49929208 | Common:3; Rare:29 | ||||
| chr19:49929395-49929579 | Common:4; Rare:65 | ||||
| chr19:49929922-49929986 | Rare:16 | ||||
| chr19:50025325-50025740 | Common:7; Rare:136 | ||||
| chr19:50377600-50377869 | Common:1; Rare:100 | ||||
| chr19:50384272-50384381 | Rare:42; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50476255-50476547 | Rare:138 | ||||
| chr19:50511137-50511228 | Rare:34 | ||||
| chr19:50511235-50511407 | Common:1; Rare:54 | ||||
| chr19:50804552-50805130 | Common:12; Rare:181 | ||||
| chr19:51108365-51108623 | Common:1; Rare:59 | ||||
| chr19:51339759-51340020 | Common:1; Rare:56 | ||||
| chr19:51366290-51366562 | Common:5; Rare:84; Clinvar (benign):2 | ||||
| chr19:51927312-51927519 | Common:1; Rare:66 |