| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:37999531-37999828 | Common:1; Rare:54 | ||||
| chr19:38004588-38004780 | Common:2; Rare:42 | ||||
| chr19:38300870-38301024 | Common:1; Rare:30 | ||||
| chr19:38304984-38305304 | Common:3; Rare:81 | ||||
| chr19:38361790-38362150 | Common:1; Rare:99 | ||||
| chr19:38497127-38497386 | Common:11; Rare:94 | ||||
| chr19:38506947-38507261 | Common:12; Rare:88; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:38543941-38544201 | Common:4; Rare:54 | ||||
| chr19:38544474-38544638 | Common:2; Rare:20 | ||||
| chr19:38545045-38545212 | Common:3; Rare:37 | ||||
| chr19:38564970-38565440 | Common:1; Rare:176; Clinvar:26; Clinvar (benign):17 | ||||
| chr19:38565460-38565750 | Common:1; Rare:111; Clinvar:16; Clinvar (benign):10 | ||||
| chr19:38596449-38596567 | Rare:28 | ||||
| chr19:38649876-38649987 | Rare:28 | ||||
| chr19:38658638-38658860 | Rare:32 |