| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:11908274-11908400 | Rare:36 | ||||
| chr18:12702678-12703069 | Common:3; Rare:154 | ||||
| chr18:12884143-12884425 | Common:4; Rare:145 | ||||
| chr18:12947694-12948098 | Common:3; Rare:113 | ||||
| chr18:12991137-12991388 | Common:1; Rare:90 | ||||
| chr18:13726439-13726729 | Common:3; Rare:112 | ||||
| chr18:21600644-21600852 | Rare:49 | ||||
| chr18:21600865-21600975 | Common:2; Rare:36 | ||||
| chr18:21612194-21612441 | Common:1; Rare:73 | ||||
| chr18:22933783-22933889 | Common:1; Rare:42 | ||||
| chr18:23437911-23438015 | Common:1; Rare:56 | ||||
| chr18:23453156-23453346 | Rare:67 | ||||
| chr18:23586426-23586550 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24397814-24398125 | Common:2; Rare:111 | ||||
| chr18:26865696-26865780 | Common:1; Rare:31 |