| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38374557-38374812 | Rare:106 | ||||
| chr19:38618975-38619240 | Common:2; Rare:73 | ||||
| chr19:38647372-38647748 | Common:3; Rare:132 | ||||
| chr19:38899528-38899954 | Rare:122 | ||||
| chr19:38930742-38930987 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39342373-39342511 | Common:2; Rare:48 | ||||
| chr19:39391009-39391418 | Common:1; Rare:159 | ||||
| chr19:39406735-39406852 | Rare:49 | ||||
| chr19:39413394-39413539 | Common:1; Rare:45 | ||||
| chr19:39435866-39436167 | Common:7; Rare:112 | ||||
| chr19:39480731-39480925 | Common:3; Rare:105; Clinvar (pathogenic):1 | ||||
| chr19:39540152-39540353 | Common:1; Rare:47 | ||||
| chr19:39830447-39830717 | Rare:98 | ||||
| chr19:39834084-39834354 | Rare:73 | ||||
| chr19:39846318-39846479 | Common:1; Rare:75 |