| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:76495194-76495405 | Common:1; Rare:64 | ||||
| chr18:76822222-76822637 | Common:11; Rare:116 | ||||
| chr18:79679269-79679581 | Common:1; Rare:153 | ||||
| chr18:79988300-79988651 | Common:3; Rare:118; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:572237-572649 | Common:3; Rare:209 | ||||
| chr19:633520-633738 | Common:8; Rare:99 | ||||
| chr19:663111-663450 | Common:3; Rare:137 | ||||
| chr19:797144-797498 | Rare:162 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:913149-913274 | Rare:40 | ||||
| chr19:984260-984406 | Rare:58 | ||||
| chr19:1021240-1021524 | Common:11; Rare:121 | ||||
| chr19:1103785-1104119 | Common:4; Rare:142 | ||||
| chr19:1132090-1132389 | Common:1; Rare:124 | ||||
| chr19:1155080-1155293 | Rare:58 |