| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:3652932-3653115 | Common:3; Rare:21 | ||||
| chr18:5237756-5237850 | Common:3; Rare:43 | ||||
| chr18:5238005-5238139 | Common:1; Rare:51 | ||||
| chr18:11852410-11852606 | Common:1; Rare:53 | ||||
| chr18:13106488-13106686 | Common:1; Rare:43 | ||||
| chr18:24015506-24015613 | Common:3; Rare:15 | ||||
| chr18:24153819-24154102 | Common:2; Rare:36 | ||||
| chr18:26038285-26038551 | Common:3; Rare:47 | ||||
| chr18:29157004-29157247 | Rare:41 | ||||
| chr18:29164121-29164343 | Common:1; Rare:39 | ||||
| chr18:35306093-35306259 | Common:2; Rare:26 | ||||
| chr18:36142284-36142413 | Rare:26; Clinvar (pathogenic):1 | ||||
| chr18:44679013-44679115 | Common:2; Rare:29 | ||||
| chr18:47164413-47164618 | Common:4; Rare:35 | ||||
| chr18:57630210-57630401 | Common:1; Rare:51 |