| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1222951-1223028 | Rare:29; Clinvar:8; Clinvar (benign):9 | ||||
| chr19:1248319-1248588 | Common:2; Rare:81 | ||||
| chr19:1260879-1261185 | Common:3; Rare:100 | ||||
| chr19:1269089-1269410 | Common:2; Rare:122 | ||||
| chr19:1354786-1355083 | Common:3; Rare:138 | ||||
| chr19:1388292-1388534 | Common:4; Rare:65; Clinvar (benign):5 | ||||
| chr19:1401307-1401644 | Common:1; Rare:108; Clinvar:14; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr19:1407229-1407417 | Common:1; Rare:96 | ||||
| chr19:1438255-1438445 | Rare:73 | ||||
| chr19:1438654-1438892 | Common:1; Rare:86; Clinvar (benign):1 | ||||
| chr19:1479158-1479252 | Rare:43 | ||||
| chr19:1490162-1490516 | Common:4; Rare:126 | ||||
| chr19:1490716-1491335 | Common:6; Rare:209 | ||||
| chr19:1495373-1495607 | Rare:97 | ||||
| chr19:1584666-1584943 | Common:2; Rare:120 |