Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:3149153-3149237 | Rare:24; Clinvar (benign):2 | ||||
chr18:5238018-5238153 | Common:1; Rare:52 | ||||
chr18:13500611-13500650 | Rare:7 | ||||
chr18:21831441-21831742 | Common:1; Rare:59 | ||||
chr18:31724625-31724680 | Rare:7 | ||||
chr18:34738650-34738899 | Common:3; Rare:42 | ||||
chr18:50973552-50973583 | Rare:4 | ||||
chr18:58256090-58256267 | Common:1; Rare:51 | ||||
chr18:73691283-73691421 | Rare:24 | ||||
chr18:75070838-75071092 | Rare:43 | ||||
chr18:76491491-76491651 | Common:3; Rare:66 | ||||
chr19:311922-312217 | Common:9; Rare:146 | ||||
chr19:2046187-2046514 | Common:3; Rare:130 | ||||
chr19:2049975-2050194 | Rare:61 | ||||
chr19:2065031-2065179 | Rare:35 |