| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:13744882-13745233 | Common:5; Rare:54 | ||||
| chr18:14110875-14111161 | Common:2; Rare:51 | ||||
| chr18:20967569-20967942 | Rare:68 | ||||
| chr18:21006350-21006786 | Common:1; Rare:92 | ||||
| chr18:21011109-21011211 | Common:1; Rare:17 | ||||
| chr18:21016876-21017159 | Common:2; Rare:46 | ||||
| chr18:21018762-21019017 | Common:1; Rare:48 | ||||
| chr18:21548355-21548390 | Rare:2 | ||||
| chr18:21744124-21744162 | Rare:4 | ||||
| chr18:21811509-21811721 | Rare:41 | ||||
| chr18:22172520-22172704 | Common:1; Rare:27 | ||||
| chr18:22174235-22174418 | Rare:30 | ||||
| chr18:22174957-22175097 | Rare:24 | ||||
| chr18:22175806-22175923 | Common:1; Rare:20 | ||||
| chr18:22182805-22183044 | Rare:57; Clinvar:1; Clinvar (benign):2 |