| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:12254237-12254370 | Common:3; Rare:43 | ||||
| chr18:12254668-12254772 | Rare:37 | ||||
| chr18:12308149-12308316 | Common:3; Rare:75 | ||||
| chr18:12702593-12703074 | Common:4; Rare:183 | ||||
| chr18:12884112-12884426 | Common:4; Rare:160 | ||||
| chr18:12947673-12948101 | Common:3; Rare:125 | ||||
| chr18:12991143-12991417 | Common:2; Rare:100 | ||||
| chr18:13726490-13726720 | Common:3; Rare:88 | ||||
| chr18:21111063-21111274 | Rare:46 | ||||
| chr18:21111778-21111938 | Common:2; Rare:49 | ||||
| chr18:21600644-21600856 | Rare:50 | ||||
| chr18:22913940-22914176 | Rare:40 | ||||
| chr18:22933141-22933385 | Common:3; Rare:73; Clinvar (benign):1 | ||||
| chr18:22933829-22933867 | Common:1; Rare:12 | ||||
| chr18:23453176-23453442 | Rare:79 |