| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12658069-12658235 | Common:5; Rare:72 | ||||
| chr18:12702626-12703155 | Common:4; Rare:206 | ||||
| chr18:13726503-13726720 | Common:3; Rare:82 | ||||
| chr18:21111598-21111923 | Common:2; Rare:106 | ||||
| chr18:21612204-21612412 | Common:1; Rare:63 | ||||
| chr18:22933789-22933902 | Common:1; Rare:45 | ||||
| chr18:24397778-24398105 | Common:2; Rare:116 | ||||
| chr18:32092367-32092724 | Common:5; Rare:165 | ||||
| chr18:34709955-34710304 | Rare:77 | ||||
| chr18:35290162-35290344 | Common:2; Rare:60 | ||||
| chr18:36129780-36129942 | Common:1; Rare:67 | ||||
| chr18:36187378-36187575 | Common:4; Rare:69 | ||||
| chr18:36828731-36829135 | Common:3; Rare:152 | ||||
| chr18:46098232-46098595 | Common:11; Rare:104; Clinvar (benign):6 | ||||
| chr18:46104137-46104378 | Common:3; Rare:66; Clinvar (benign):1 |