| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51029439-51029839 | Common:1; Rare:93 | ||||
| chr18:51029900-51030300 | Rare:540; Clinvar:14 | ||||
| chr18:51030522-51030922 | Common:5; Rare:237; Clinvar:5; Clinvar (benign):10 | ||||
| chr18:51195550-51196302 | Common:4; Rare:288 | ||||
| chr18:51196576-51197539 | Common:31; Rare:893 | ||||
| chr18:51197510-51198101 | Rare:928 | ||||
| chr18:54224491-54224959 | Common:4; Rare:356 | ||||
| chr18:54269200-54269835 | Common:27; Rare:815 | ||||
| chr18:54269870-54270380 | Common:4; Rare:193 | ||||
| chr18:54357327-54357727 | Common:3; Rare:85 | ||||
| chr18:54357674-54358504 | Common:47; Rare:507 | ||||
| chr18:54358506-54358608 | Common:1; Rare:24 | ||||
| chr18:54717625-54718025 | Common:1; Rare:98 | ||||
| chr18:54828070-54828930 | Common:15; Rare:503 | ||||
| chr18:54959280-54959680 | Common:5; Rare:155 |