| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:22933277-22933385 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr18:22933764-22933912 | Common:1; Rare:61 | ||||
| chr18:23453156-23453342 | Rare:66 | ||||
| chr18:23503300-23503576 | Common:2; Rare:103 | ||||
| chr18:23586400-23586541 | Common:2; Rare:65; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:24138942-24139063 | Common:2; Rare:43 | ||||
| chr18:24397758-24397988 | Common:2; Rare:92 | ||||
| chr18:24426620-24426725 | Common:2; Rare:44 | ||||
| chr18:26657382-26657481 | Rare:25 | ||||
| chr18:26865690-26865845 | Common:1; Rare:43 | ||||
| chr18:28176988-28177183 | Common:3; Rare:98 | ||||
| chr18:32092384-32092745 | Common:5; Rare:161 | ||||
| chr18:33578216-33578547 | Common:4; Rare:91 | ||||
| chr18:34048529-34048690 | Rare:25 | ||||
| chr18:34221895-34222006 | Common:1; Rare:17 |