Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:42455993-42456124 | Rare:45 | ||||
chr1:42456219-42456756 | Common:3; Rare:176 | ||||
chr1:42456901-42456969 | Rare:24 | ||||
chr1:42658275-42658477 | Common:2; Rare:59 | ||||
chr1:42682132-42682442 | Common:2; Rare:81 | ||||
chr1:42682606-42682730 | Common:1; Rare:51 | ||||
chr1:42683257-42683465 | Common:3; Rare:85 | ||||
chr1:42766528-42766726 | Rare:51; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:42766976-42767313 | Common:4; Rare:116; Clinvar (benign):1 | ||||
chr1:42817004-42817145 | Common:1; Rare:35 | ||||
chr1:42817198-42817676 | Rare:132 | ||||
chr1:42846391-42846638 | Common:1; Rare:69 | ||||
chr1:42958839-42959042 | Common:3; Rare:55; Clinvar:5; Clinvar (benign):4 | ||||
chr1:43172135-43172362 | Common:3; Rare:94 | ||||
chr1:43270940-43270978 | Rare:6 |