| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:76495201-76495522 | Common:2; Rare:88 | ||||
| chr18:76822236-76822636 | Common:11; Rare:112 | ||||
| chr18:77131332-77131571 | Common:2; Rare:52 | ||||
| chr18:77133680-77133849 | Rare:41 | ||||
| chr18:79988294-79988640 | Common:3; Rare:117; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:572237-572649 | Common:3; Rare:209 | ||||
| chr19:663117-663430 | Common:3; Rare:123 | ||||
| chr19:797113-797493 | Rare:169 | ||||
| chr19:804683-804934 | Rare:78 | ||||
| chr19:893158-893484 | Common:3; Rare:139 | ||||
| chr19:913144-913289 | Rare:46 | ||||
| chr19:984232-984406 | Rare:69 | ||||
| chr19:1021207-1021575 | Common:15; Rare:175 | ||||
| chr19:1066956-1067187 | Common:1; Rare:57 | ||||
| chr19:1103749-1104126 | Common:7; Rare:157 |