| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12419832-12419911 | Common:1; Rare:13 | ||||
| chr18:12702627-12703087 | Common:3; Rare:178 | ||||
| chr18:12884159-12884425 | Common:4; Rare:130 | ||||
| chr18:12947640-12948061 | Common:3; Rare:107 | ||||
| chr18:12991108-12991420 | Common:2; Rare:116 | ||||
| chr18:13464894-13465043 | Rare:25 | ||||
| chr18:13612248-13612636 | Common:2; Rare:76 | ||||
| chr18:13726456-13726741 | Common:3; Rare:109 | ||||
| chr18:14132390-14132570 | Common:3; Rare:51 | ||||
| chr18:21111625-21112021 | Common:3; Rare:133 | ||||
| chr18:21600621-21600852 | Rare:55 | ||||
| chr18:21600948-21601141 | Rare:35 | ||||
| chr18:21612179-21612441 | Common:1; Rare:78 | ||||
| chr18:21704652-21704991 | Common:3; Rare:106 | ||||
| chr18:22933230-22933426 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):2 |