Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:31846541-31846818 | Common:1; Rare:94 | ||||
chr13:32211602-32211890 | Common:2; Rare:41 | ||||
chr13:33016979-33017076 | Rare:40; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr13:35857833-35858068 | Common:3; Rare:46 | ||||
chr13:40921646-40921941 | Common:5; Rare:76 | ||||
chr13:42271241-42271524 | Common:4; Rare:74 | ||||
chr13:48413060-48413159 | Rare:15 | ||||
chr13:50048967-50049249 | Common:1; Rare:60 | ||||
chr13:52194370-52194472 | Rare:34 | ||||
chr13:52600327-52600514 | Common:3; Rare:65 | ||||
chr13:52617317-52617541 | Common:1; Rare:55 | ||||
chr13:57629910-57630136 | Common:1; Rare:67 | ||||
chr13:70107767-70107868 | Common:1; Rare:32 | ||||
chr13:71616743-71616806 | Rare:8 | ||||
chr13:71752334-71752650 | Common:1; Rare:40 |