| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:54828338-54828489 | Rare:35 | ||||
| chr18:55321717-55321921 | Rare:45 | ||||
| chr18:55401659-55401990 | Rare:60 | ||||
| chr18:55422309-55422591 | Common:1; Rare:51 | ||||
| chr18:55586055-55586190 | Common:1; Rare:48 | ||||
| chr18:55589701-55589996 | Common:2; Rare:94 | ||||
| chr18:56651275-56651435 | Common:2; Rare:41 | ||||
| chr18:56651610-56651705 | Common:3; Rare:22 | ||||
| chr18:57621718-57621971 | Common:3; Rare:90 | ||||
| chr18:59359192-59359517 | Common:4; Rare:149; Clinvar:2; Clinvar (benign):1 | ||||
| chr18:59697632-59697885 | Common:1; Rare:64 | ||||
| chr18:59899849-59900006 | Common:3; Rare:48 | ||||
| chr18:62186928-62187334 | Common:5; Rare:111 | ||||
| chr18:62715166-62715487 | Common:3; Rare:88 | ||||
| chr18:63319981-63320167 | Common:1; Rare:60 |