| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:50476226-50476557 | Common:1; Rare:154 | ||||
| chr19:50511137-50511304 | Rare:59 | ||||
| chr19:50804572-50804748 | Common:5; Rare:60 | ||||
| chr19:51001112-51001230 | Common:2; Rare:37 | ||||
| chr19:51019361-51019598 | Common:1; Rare:63 | ||||
| chr19:51019675-51019906 | Common:4; Rare:41 | ||||
| chr19:51024400-51024638 | Common:4; Rare:73 | ||||
| chr19:51026537-51026915 | Common:2; Rare:88 | ||||
| chr19:51027063-51027169 | Rare:19 | ||||
| chr19:51027172-51027240 | Rare:15 | ||||
| chr19:51027477-51027714 | Common:1; Rare:48 | ||||
| chr19:51342102-51342203 | Common:1; Rare:18 | ||||
| chr19:51366271-51366537 | Common:5; Rare:79; Clinvar (benign):2 | ||||
| chr19:51887874-51888035 | Rare:56 | ||||
| chr19:52008182-52008332 | Rare:44 |