| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:77133691-77133948 | Common:1; Rare:54 | ||||
| chr18:79400128-79400329 | Common:2; Rare:71 | ||||
| chr18:79679276-79679610 | Common:1; Rare:166 | ||||
| chr18:79951651-79951866 | Common:4; Rare:83 | ||||
| chr18:79964545-79964742 | Common:2; Rare:61 | ||||
| chr18:79988290-79988640 | Common:3; Rare:117; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:507479-507509 | Rare:9 | ||||
| chr19:571740-571870 | Common:2; Rare:26 | ||||
| chr19:572289-572701 | Common:4; Rare:201 | ||||
| chr19:582303-582582 | Common:3; Rare:100 | ||||
| chr19:632955-633054 | Common:2; Rare:33 | ||||
| chr19:633486-633568 | Common:6; Rare:66 | ||||
| chr19:663126-663380 | Common:3; Rare:97 | ||||
| chr19:750978-751168 | Common:2; Rare:38 | ||||
| chr19:797083-797423 | Rare:131 |