| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50967884-50968054 | Rare:58 | ||||
| chr18:51030054-51030252 | Rare:68; Clinvar:1 | ||||
| chr18:54357838-54357964 | Common:5; Rare:39 | ||||
| chr18:54828361-54828944 | Common:5; Rare:124 | ||||
| chr18:54959037-54959065 | Rare:5 | ||||
| chr18:54959311-54959511 | Common:1; Rare:51 | ||||
| chr18:55321713-55321920 | Rare:45 | ||||
| chr18:55422316-55422624 | Common:1; Rare:52 | ||||
| chr18:55588599-55588623 | Rare:4 | ||||
| chr18:55589704-55590032 | Common:2; Rare:108 | ||||
| chr18:56651132-56651559 | Common:5; Rare:105 | ||||
| chr18:56651620-56651705 | Common:3; Rare:20 | ||||
| chr18:57621706-57621949 | Common:3; Rare:85 | ||||
| chr18:57740302-57740502 | Common:1; Rare:35 | ||||
| chr18:57802989-57803578 | Common:6; Rare:151; Clinvar:2; Clinvar (benign):2 |