| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54357839-54357973 | Common:5; Rare:42 | ||||
| chr18:54358416-54358593 | Common:1; Rare:35 | ||||
| chr18:54828591-54828658 | Common:1; Rare:7 | ||||
| chr18:54959331-54959530 | Common:2; Rare:49 | ||||
| chr18:55321752-55321955 | Rare:47 | ||||
| chr18:55322337-55322602 | Rare:59 | ||||
| chr18:55401955-55402139 | Common:1; Rare:35 | ||||
| chr18:55587649-55587999 | Rare:83 | ||||
| chr18:55588099-55588248 | Rare:34; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:56638547-56638978 | Common:7; Rare:148 | ||||
| chr18:56651124-56651428 | Common:4; Rare:80 | ||||
| chr18:57435217-57435428 | Rare:49 | ||||
| chr18:57586509-57586586 | Rare:29 | ||||
| chr18:57586597-57586746 | Rare:46 | ||||
| chr18:57586893-57587059 | Rare:26 |