Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:36187413-36187530 | Common:2; Rare:45 | ||||
chr18:36828741-36829132 | Common:3; Rare:151 | ||||
chr18:45967261-45967465 | Rare:74 | ||||
chr18:46098218-46098550 | Common:11; Rare:99; Clinvar (benign):6 | ||||
chr18:46104135-46104406 | Common:4; Rare:79; Clinvar (benign):1 | ||||
chr18:49561879-49562101 | Rare:58 | ||||
chr18:49813833-49814120 | Common:1; Rare:120 | ||||
chr18:50878832-50879228 | Common:4; Rare:130 | ||||
chr18:54357856-54357973 | Common:5; Rare:35 | ||||
chr18:55589809-55589948 | Common:2; Rare:48 | ||||
chr18:56651133-56651371 | Common:3; Rare:59 | ||||
chr18:62186948-62187320 | Common:5; Rare:104 | ||||
chr18:63422381-63422643 | Common:1; Rare:68 | ||||
chr18:68714987-68715216 | Common:3; Rare:99 | ||||
chr18:70205648-70205774 | Common:3; Rare:53; Clinvar (benign):2 |