| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:63422344-63422760 | Common:2; Rare:124 | ||||
| chr18:68714982-68715335 | Common:7; Rare:145 | ||||
| chr18:70205644-70205814 | Common:3; Rare:71; Clinvar (benign):2 | ||||
| chr18:70206000-70206142 | Rare:53 | ||||
| chr18:74148353-74148619 | Common:1; Rare:76 | ||||
| chr18:74291906-74292295 | Common:5; Rare:116 | ||||
| chr18:74496046-74496416 | Common:4; Rare:119 | ||||
| chr18:74597380-74597434 | Common:1; Rare:11 | ||||
| chr18:74597584-74597929 | Common:2; Rare:95 | ||||
| chr18:75210808-75210874 | Rare:17; Clinvar:1 | ||||
| chr18:76495164-76495538 | Common:2; Rare:97 | ||||
| chr18:79679224-79679587 | Common:3; Rare:175 | ||||
| chr18:79988274-79988638 | Common:3; Rare:119; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:344790-344955 | Common:3; Rare:60 | ||||
| chr19:409109-409317 | Common:2; Rare:71 |