| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:45496959-45497278 | Common:3; Rare:96 | ||||
| chr19:45507386-45507535 | Rare:49 | ||||
| chr19:45692457-45692691 | Common:1; Rare:53 | ||||
| chr19:45779444-45779803 | Common:2; Rare:125 | ||||
| chr19:45863125-45863364 | Common:3; Rare:77 | ||||
| chr19:46298120-46298456 | Common:5; Rare:80 | ||||
| chr19:46346951-46347181 | Common:3; Rare:81 | ||||
| chr19:46495846-46495940 | Rare:30 | ||||
| chr19:46600913-46601420 | Common:5; Rare:175; Clinvar (benign):1 | ||||
| chr19:46608290-46608574 | Common:1; Rare:66; Clinvar (benign):6 | ||||
| chr19:46661025-46661202 | Rare:46 | ||||
| chr19:46746306-46746572 | Common:4; Rare:83 | ||||
| chr19:47112473-47112779 | Common:2; Rare:91 | ||||
| chr19:47112799-47112913 | Common:1; Rare:30 | ||||
| chr19:47113107-47113409 | Common:2; Rare:79 |