| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18941130-18941510 | Common:5; Rare:105 | ||||
| chr19:19033431-19033649 | Common:2; Rare:74 | ||||
| chr19:19033804-19033914 | Common:1; Rare:29 | ||||
| chr19:19063675-19064075 | Common:1; Rare:200 | ||||
| chr19:19105662-19105852 | Common:1; Rare:66; Clinvar (pathogenic):1 | ||||
| chr19:19138446-19138663 | Common:2; Rare:57 | ||||
| chr19:19192100-19192347 | Common:2; Rare:69; Clinvar (benign):1 | ||||
| chr19:19192567-19192970 | Common:2; Rare:106 | ||||
| chr19:19203320-19203640 | Rare:94 | ||||
| chr19:19261610-19261980 | Common:3; Rare:98 | ||||
| chr19:19272902-19273152 | Common:4; Rare:60 | ||||
| chr19:19320458-19320871 | Common:4; Rare:157 | ||||
| chr19:19385416-19385755 | Common:1; Rare:81 | ||||
| chr19:19405500-19405831 | Common:4; Rare:115 | ||||
| chr19:19464410-19464760 | Common:2; Rare:64 |