| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13726234-13726301 | Rare:14 | ||||
| chr18:13726339-13727007 | Common:8; Rare:198 | ||||
| chr18:14132415-14132570 | Common:2; Rare:39 | ||||
| chr18:21111661-21111977 | Common:2; Rare:106 | ||||
| chr18:21600549-21600899 | Rare:95 | ||||
| chr18:21612202-21612441 | Common:1; Rare:71 | ||||
| chr18:21704670-21704984 | Common:3; Rare:100 | ||||
| chr18:22933280-22933446 | Common:2; Rare:69; Clinvar:4; Clinvar (benign):2 | ||||
| chr18:22933756-22933919 | Common:1; Rare:69 | ||||
| chr18:23134406-23134597 | Common:3; Rare:32 | ||||
| chr18:23155618-23155852 | Common:1; Rare:41 | ||||
| chr18:23156084-23156264 | Common:1; Rare:35 | ||||
| chr18:23453172-23453346 | Rare:59 | ||||
| chr18:23503298-23503554 | Common:2; Rare:94 | ||||
| chr18:23586379-23586537 | Common:2; Rare:70; Clinvar:3; Clinvar (benign):1 |