| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50281660-50282020 | Common:3; Rare:118 | ||||
| chr18:50287634-50287975 | Common:2; Rare:102 | ||||
| chr18:50374875-50375199 | Common:4; Rare:98 | ||||
| chr18:50559619-50560094 | Common:7; Rare:171 | ||||
| chr18:50560456-50560606 | Common:1; Rare:37 | ||||
| chr18:50878862-50879206 | Common:4; Rare:114 | ||||
| chr18:50967867-50968219 | Common:1; Rare:119 | ||||
| chr18:51029957-51030277 | Rare:101; Clinvar:3 | ||||
| chr18:51030550-51030860 | Common:1; Rare:108; Clinvar:2; Clinvar (benign):4 | ||||
| chr18:51197533-51198026 | Rare:152 | ||||
| chr18:52339940-52340600 | Common:4; Rare:149 | ||||
| chr18:54224495-54224868 | Common:1; Rare:104 | ||||
| chr18:54269398-54269628 | Common:2; Rare:102 | ||||
| chr18:54357758-54357982 | Common:8; Rare:69 | ||||
| chr18:54358178-54358365 | Common:1; Rare:29 |