| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586407-23586528 | Common:2; Rare:56; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24397795-24397958 | Common:1; Rare:72 | ||||
| chr18:24426593-24426739 | Common:3; Rare:59 | ||||
| chr18:26657382-26657488 | Rare:28 | ||||
| chr18:26865678-26865818 | Common:1; Rare:45 | ||||
| chr18:31943098-31943381 | Common:7; Rare:93 | ||||
| chr18:32092384-32092727 | Common:5; Rare:156 | ||||
| chr18:33578216-33578528 | Common:4; Rare:88 | ||||
| chr18:34048545-34048666 | Rare:17 | ||||
| chr18:34221895-34221995 | Common:1; Rare:15 | ||||
| chr18:34222061-34222404 | Common:2; Rare:74 | ||||
| chr18:34224793-34225060 | Common:3; Rare:53 | ||||
| chr18:35041268-35041476 | Rare:78 | ||||
| chr18:35240949-35241069 | Rare:43 | ||||
| chr18:35290193-35290384 | Common:2; Rare:68 |