| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:46661168-46661449 | Rare:78 | ||||
| chr19:46713781-46714049 | Common:1; Rare:79 | ||||
| chr19:46714055-46714706 | Common:4; Rare:143 | ||||
| chr19:46717047-46717282 | Common:3; Rare:75 | ||||
| chr19:46745622-46745652 | Rare:4 | ||||
| chr19:46745797-46746116 | Common:3; Rare:81; Clinvar (benign):3 | ||||
| chr19:46746398-46746576 | Common:3; Rare:62 | ||||
| chr19:46784410-46784435 | Rare:3 | ||||
| chr19:46784716-46785093 | Common:1; Rare:85 | ||||
| chr19:46787257-46787674 | Common:1; Rare:126 | ||||
| chr19:46788301-46788336 | Common:2; Rare:8 | ||||
| chr19:46788514-46788888 | Common:2; Rare:82 | ||||
| chr19:46850227-46850461 | Rare:32 | ||||
| chr19:46850662-46850717 | Rare:16 | ||||
| chr19:47035872-47036156 | Rare:98 |