| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:68714987-68715296 | Common:7; Rare:132 | ||||
| chr18:70205659-70205764 | Common:2; Rare:46; Clinvar (benign):2 | ||||
| chr18:74148358-74148590 | Common:1; Rare:67 | ||||
| chr18:74597359-74597478 | Common:1; Rare:31 | ||||
| chr18:74597554-74597929 | Common:2; Rare:103 | ||||
| chr18:76822227-76822621 | Common:11; Rare:111 | ||||
| chr18:77132721-77132779 | Common:1; Rare:18 | ||||
| chr18:79400203-79400340 | Common:2; Rare:56 | ||||
| chr18:79679269-79679584 | Common:1; Rare:155 | ||||
| chr18:79988356-79988661 | Common:4; Rare:110; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572311-572649 | Common:1; Rare:178 | ||||
| chr19:633497-633724 | Common:8; Rare:113 | ||||
| chr19:676149-676397 | Common:4; Rare:80 | ||||
| chr19:797206-797459 | Rare:110 | ||||
| chr19:893165-893484 | Common:3; Rare:133 |