| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45792693-45793101 | Common:4; Rare:260 | ||||
| chr19:45862058-45862458 | Common:2; Rare:85 | ||||
| chr19:45862360-45862780 | Common:3; Rare:160 | ||||
| chr19:45863027-45863459 | Common:26; Rare:668 | ||||
| chr19:45864020-45864427 | Common:14; Rare:345 | ||||
| chr19:45885753-45886710 | Common:22; Rare:564 | ||||
| chr19:45902527-45903033 | Common:20; Rare:650 | ||||
| chr19:45995004-45995530 | Common:5; Rare:535 | ||||
| chr19:46160000-46160431 | Common:5; Rare:153 | ||||
| chr19:46346438-46347182 | Common:23; Rare:594 | ||||
| chr19:46347279-46347708 | Common:2; Rare:177 | ||||
| chr19:46413404-46414182 | Common:11; Rare:616 | ||||
| chr19:46470981-46472001 | Common:51; Rare:671 | ||||
| chr19:46471985-46472344 | Common:4; Rare:79 | ||||
| chr19:46600432-46601442 | Common:31; Rare:1277; Clinvar (benign):6 |