| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:49850929-49851022 | Common:1; Rare:34 | ||||
| chr19:49867542-49867643 | Common:2; Rare:34 | ||||
| chr19:49877313-49877541 | Rare:49 | ||||
| chr19:49929377-49929594 | Common:4; Rare:73 | ||||
| chr19:49929918-49930219 | Common:1; Rare:72 | ||||
| chr19:50025335-50025722 | Common:7; Rare:125 | ||||
| chr19:50384005-50384381 | Common:3; Rare:162; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:50432654-50433064 | Common:4; Rare:97 | ||||
| chr19:50476375-50476542 | Rare:78 | ||||
| chr19:50626126-50626198 | Rare:13 | ||||
| chr19:50804953-50805106 | Common:2; Rare:47 | ||||
| chr19:51366335-51366544 | Common:5; Rare:54; Clinvar (benign):2 | ||||
| chr19:51986821-51987032 | Common:2; Rare:55 | ||||
| chr19:52008182-52008359 | Rare:52 | ||||
| chr19:52028336-52028471 | Common:3; Rare:29 |