Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26279840-26280161 | Rare:175 | ||||
chr1:26306361-26306462 | Rare:18 | ||||
chr1:26306530-26306916 | Common:14; Rare:107 | ||||
chr1:26335991-26336140 | Rare:35 | ||||
chr1:26336334-26336505 | Common:1; Rare:60 | ||||
chr1:26336529-26336948 | Common:3; Rare:167 | ||||
chr1:26431976-26432445 | Common:5; Rare:114; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472043-26472301 | Common:1; Rare:64 | ||||
chr1:26472333-26473297 | Common:10; Rare:387 | ||||
chr1:26529686-26529865 | Rare:59 | ||||
chr1:26529968-26530154 | Common:3; Rare:49 | ||||
chr1:26531210-26531545 | Common:3; Rare:62 | ||||
chr1:26531699-26531721 | Rare:5 | ||||
chr1:26531726-26531972 | Common:2; Rare:52 | ||||
chr1:26695598-26695801 | Rare:68 |