| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:21111614-21112113 | Common:3; Rare:156 | ||||
| chr18:21600625-21600852 | Rare:54 | ||||
| chr18:22169452-22169589 | Rare:38 | ||||
| chr18:22933277-22933426 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):2 | ||||
| chr18:22933765-22933889 | Common:1; Rare:49 | ||||
| chr18:23453115-23453370 | Rare:92 | ||||
| chr18:23503298-23503576 | Common:2; Rare:103 | ||||
| chr18:23586396-23586541 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:23884334-23884685 | Common:1; Rare:61 | ||||
| chr18:25351033-25351145 | Rare:38 | ||||
| chr18:25352004-25352392 | Common:1; Rare:146 | ||||
| chr18:28177006-28177314 | Common:3; Rare:147 | ||||
| chr18:31943098-31943380 | Common:7; Rare:92 | ||||
| chr18:32091820-32091969 | Common:3; Rare:52 | ||||
| chr18:32092384-32092732 | Common:5; Rare:157 |