| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:77087440-77087486 | Common:3; Rare:12 | ||||
| chr18:77250912-77251041 | Rare:39 | ||||
| chr18:79400000-79400338 | Common:6; Rare:108 | ||||
| chr18:79679210-79679587 | Common:3; Rare:177 | ||||
| chr18:79964518-79964742 | Common:2; Rare:70 | ||||
| chr18:79988268-79988645 | Common:3; Rare:122; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:344786-344955 | Common:3; Rare:61 | ||||
| chr19:507119-507408 | Common:2; Rare:89 | ||||
| chr19:572322-572701 | Common:1; Rare:187 | ||||
| chr19:582305-582582 | Common:3; Rare:100 | ||||
| chr19:633497-633765 | Common:8; Rare:124 | ||||
| chr19:663117-663430 | Common:3; Rare:123 | ||||
| chr19:676264-676424 | Common:4; Rare:66 | ||||
| chr19:680590-680752 | Common:2; Rare:53 | ||||
| chr19:708792-709141 | Common:3; Rare:95 |