Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:123584336-123584622 | Common:5; Rare:101 | ||||
chr12:123601934-123602156 | Common:4; Rare:70 | ||||
chr12:123633597-123633851 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
chr12:130871697-130872110 | Common:4; Rare:171 | ||||
chr13:20773941-20774062 | Common:1; Rare:38 | ||||
chr13:21140223-21140636 | Rare:162 | ||||
chr13:21176473-21176711 | Common:2; Rare:106 | ||||
chr13:23889327-23889455 | Rare:45 | ||||
chr13:24160475-24160764 | Rare:81 | ||||
chr13:24512738-24512870 | Common:3; Rare:39 | ||||
chr13:24922790-24922989 | Rare:55; Clinvar:1 | ||||
chr13:25301485-25301724 | Common:1; Rare:87 | ||||
chr13:26221792-26221918 | Rare:32 | ||||
chr13:26222246-26222554 | Common:5; Rare:78 | ||||
chr13:27251251-27251617 | Common:5; Rare:109 |