| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48501470-48501730 | Common:2; Rare:102 | ||||
| chr19:48513910-48514294 | Common:3; Rare:97 | ||||
| chr19:48558502-48558707 | Common:2; Rare:45 | ||||
| chr19:48568260-48568690 | Common:12; Rare:134 | ||||
| chr19:48588900-48589120 | Common:1; Rare:60 | ||||
| chr19:48660960-48661400 | Common:3; Rare:155 | ||||
| chr19:48714040-48714690 | Common:6; Rare:262 | ||||
| chr19:48729350-48729940 | Common:6; Rare:282 | ||||
| chr19:48780670-48780976 | Common:3; Rare:93 | ||||
| chr19:48873021-48873353 | Common:4; Rare:76 | ||||
| chr19:48912800-48913170 | Common:2; Rare:233 | ||||
| chr19:48963833-48964002 | Common:2; Rare:52 | ||||
| chr19:49006801-49007323 | Common:2; Rare:220 | ||||
| chr19:49765550-49765865 | Common:1; Rare:71 | ||||
| chr19:50401452-50402500 | Common:13; Rare:409; Clinvar:84; Clinvar (benign):95 |