| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39996924-39997079 | Common:5; Rare:47 | ||||
| chr19:40056157-40056262 | Rare:15 | ||||
| chr19:40348393-40348724 | Common:4; Rare:105 | ||||
| chr19:40614016-40614349 | Common:2; Rare:88; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:40716861-40717112 | Common:1; Rare:85 | ||||
| chr19:40718222-40718252 | Rare:9 | ||||
| chr19:41218854-41218965 | Common:1; Rare:23 | ||||
| chr19:41262375-41262566 | Rare:34 | ||||
| chr19:41353741-41354079 | Common:2; Rare:106 | ||||
| chr19:41755365-41755596 | Rare:40 | ||||
| chr19:41959260-41959456 | Common:1; Rare:65 | ||||
| chr19:42075840-42076199 | Rare:98 | ||||
| chr19:42389795-42390014 | Rare:39 | ||||
| chr19:42412404-42412622 | Common:1; Rare:36 | ||||
| chr19:42442903-42442922 | Rare:4 |