| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:44747412-44747743 | Common:1; Rare:63 | ||||
| chr19:44748032-44748196 | Rare:33 | ||||
| chr19:44757440-44757717 | Common:1; Rare:62 | ||||
| chr19:44808972-44809150 | Rare:67 | ||||
| chr19:44905575-44905865 | Common:2; Rare:90; Clinvar:1 | ||||
| chr19:44914647-44914945 | Common:1; Rare:80 | ||||
| chr19:44954896-44955017 | Common:2; Rare:34 | ||||
| chr19:44955255-44955448 | Common:2; Rare:59 | ||||
| chr19:45038951-45039105 | Rare:55 | ||||
| chr19:45178629-45178800 | Common:4; Rare:40; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:45406339-45406676 | Common:1; Rare:82 | ||||
| chr19:45423486-45423821 | Common:3; Rare:69; Clinvar (benign):1 | ||||
| chr19:45450733-45451027 | Common:4; Rare:56 | ||||
| chr19:45469252-45469476 | Rare:68 | ||||
| chr19:45496972-45497278 | Common:3; Rare:92 |