| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:46072234-46072319 | Common:1; Rare:19 | ||||
| chr18:46098025-46098102 | Common:2; Rare:32 | ||||
| chr18:46098211-46098614 | Common:11; Rare:120; Clinvar (benign):6 | ||||
| chr18:46104191-46104458 | Common:3; Rare:77 | ||||
| chr18:46173423-46173645 | Rare:58 | ||||
| chr18:46173869-46174233 | Common:2; Rare:88 | ||||
| chr18:46333800-46334018 | Common:2; Rare:61 | ||||
| chr18:46756709-46756948 | Common:2; Rare:77 | ||||
| chr18:46917394-46917689 | Common:2; Rare:121 | ||||
| chr18:46946593-46946806 | Common:1; Rare:35 | ||||
| chr18:47150102-47150303 | Common:2; Rare:70 | ||||
| chr18:47150405-47150657 | Common:4; Rare:102 | ||||
| chr18:47930356-47930684 | Common:1; Rare:145 | ||||
| chr18:47930997-47931412 | Common:2; Rare:154 | ||||
| chr18:47931513-47931900 | Common:3; Rare:95 |