| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23586391-23586530 | Common:2; Rare:62; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24014665-24014826 | Rare:46 | ||||
| chr18:24271632-24271715 | Rare:23 | ||||
| chr18:24397763-24397987 | Common:2; Rare:90 | ||||
| chr18:24426611-24426787 | Common:3; Rare:66 | ||||
| chr18:25352104-25352438 | Common:2; Rare:133 | ||||
| chr18:26091100-26091326 | Common:2; Rare:60 | ||||
| chr18:26226246-26226529 | Common:5; Rare:108 | ||||
| chr18:28176971-28177418 | Common:3; Rare:213 | ||||
| chr18:31943084-31943386 | Common:7; Rare:100 | ||||
| chr18:32091610-32091933 | Common:8; Rare:91 | ||||
| chr18:32092366-32092732 | Common:5; Rare:166 | ||||
| chr18:35240917-35241119 | Common:2; Rare:73 | ||||
| chr18:35290178-35290394 | Common:2; Rare:76 | ||||
| chr18:35972469-35972794 | Common:3; Rare:114 |