Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:45967265-45967465 | Rare:69 | ||||
chr18:46098175-46098592 | Common:11; Rare:129; Clinvar (benign):8 | ||||
chr18:46104135-46104408 | Common:4; Rare:80; Clinvar (benign):1 | ||||
chr18:46756795-46756961 | Common:2; Rare:49 | ||||
chr18:49487122-49487328 | Common:3; Rare:78 | ||||
chr18:49813826-49814128 | Common:1; Rare:126 | ||||
chr18:50281758-50281897 | Rare:54 | ||||
chr18:50878943-50879254 | Common:4; Rare:102 | ||||
chr18:51030048-51030238 | Rare:63 | ||||
chr18:54269493-54269617 | Common:1; Rare:67 | ||||
chr18:56651124-56651388 | Common:3; Rare:64 | ||||
chr18:56890754-56890927 | Rare:31 | ||||
chr18:57621706-57621965 | Common:3; Rare:91 | ||||
chr18:58628766-58629209 | Common:4; Rare:73 | ||||
chr18:62186945-62187334 | Common:5; Rare:106 |