| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1354584-1355074 | Common:4; Rare:207 | ||||
| chr19:1383264-1383560 | Common:2; Rare:145 | ||||
| chr19:1383794-1383958 | Rare:65; Clinvar (benign):2 | ||||
| chr19:1401481-1401686 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:1407146-1407749 | Common:3; Rare:234 | ||||
| chr19:1407766-1407879 | Rare:22 | ||||
| chr19:1414982-1415279 | Rare:62 | ||||
| chr19:1415302-1415339 | Rare:2 | ||||
| chr19:1438225-1438504 | Common:1; Rare:117 | ||||
| chr19:1445744-1445844 | Common:3; Rare:20 | ||||
| chr19:1445994-1446274 | Common:2; Rare:74 | ||||
| chr19:1479143-1479386 | Common:1; Rare:103 | ||||
| chr19:1479532-1479666 | Common:1; Rare:34 | ||||
| chr19:1490293-1490510 | Common:3; Rare:77 | ||||
| chr19:1490648-1490703 | Common:1; Rare:11 |