Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:130913195-130913508 | Common:1; Rare:58 | ||||
chr7:134432377-134432524 | Rare:53 | ||||
chr7:156950512-156950584 | Common:2; Rare:25 | ||||
chr8:23298098-23298188 | Rare:32 | ||||
chr8:61577900-61578142 | Common:3; Rare:26 | ||||
chr8:126557712-126557883 | Rare:43 | ||||
chr8:127737652-127737787 | Common:1; Rare:40 | ||||
chr8:128322958-128323132 | Common:1; Rare:27 | ||||
chr8:143937414-143937551 | Rare:39 | ||||
chr8:145002812-145002957 | Common:1; Rare:47 | ||||
chr9:693477-693737 | Rare:59 | ||||
chr9:21559828-21559927 | Rare:60 | ||||
chr9:22237884-22238161 | Common:1; Rare:46 | ||||
chr9:33026616-33026985 | Common:2; Rare:105 | ||||
chr9:35657601-35657764 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 |