| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50287614-50287746 | Common:1; Rare:48 | ||||
| chr18:50878959-50879228 | Common:4; Rare:90 | ||||
| chr18:51030064-51030222 | Rare:51 | ||||
| chr18:52340250-52340287 | Rare:11 | ||||
| chr18:52340622-52340745 | Common:1; Rare:30 | ||||
| chr18:54357392-54357657 | Common:2; Rare:56 | ||||
| chr18:54357860-54358010 | Common:6; Rare:48 | ||||
| chr18:55321382-55321561 | Rare:36 | ||||
| chr18:55321617-55321942 | Rare:75 | ||||
| chr18:55321957-55322059 | Common:1; Rare:26 | ||||
| chr18:55400994-55401332 | Rare:52 | ||||
| chr18:55401365-55401406 | Common:1; Rare:5 | ||||
| chr18:55401619-55401795 | Rare:35 | ||||
| chr18:55403588-55403724 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr18:55422641-55423011 | Common:1; Rare:59 |