| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54357873-54357903 | Rare:9 | ||||
| chr18:54959375-54959561 | Common:2; Rare:49 | ||||
| chr18:55588120-55588319 | Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:56651125-56651388 | Common:3; Rare:64 | ||||
| chr18:57586596-57586855 | Rare:70 | ||||
| chr18:57621718-57621981 | Common:3; Rare:93 | ||||
| chr18:59697638-59697852 | Common:1; Rare:59 | ||||
| chr18:62186915-62187320 | Common:5; Rare:114 | ||||
| chr18:63367099-63367328 | Common:1; Rare:81 | ||||
| chr18:63422344-63422648 | Common:1; Rare:80 | ||||
| chr18:68714987-68715271 | Common:6; Rare:125 | ||||
| chr18:70205638-70205765 | Common:2; Rare:58; Clinvar (benign):2 | ||||
| chr18:74291853-74292267 | Common:4; Rare:125; Clinvar:1 | ||||
| chr18:74597601-74597897 | Common:2; Rare:78 | ||||
| chr19:572226-572618 | Common:4; Rare:186 |