Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40692062-40692299 | Common:1; Rare:69 | ||||
chr1:42335157-42335366 | Common:5; Rare:105 | ||||
chr1:42456010-42456583 | Common:1; Rare:168 | ||||
chr1:42658314-42658466 | Rare:46 | ||||
chr1:42682117-42682465 | Common:2; Rare:98 | ||||
chr1:42683255-42683465 | Common:3; Rare:86 | ||||
chr1:42766976-42767314 | Common:5; Rare:116; Clinvar (benign):1 | ||||
chr1:42817009-42817136 | Common:1; Rare:32 | ||||
chr1:42846401-42846636 | Common:1; Rare:65 | ||||
chr1:42958827-42959084 | Common:4; Rare:72; Clinvar:6; Clinvar (benign):4 | ||||
chr1:43172194-43172335 | Common:1; Rare:61 | ||||
chr1:43358829-43359006 | Rare:45 | ||||
chr1:43367937-43368197 | Rare:63 | ||||
chr1:43389757-43389945 | Common:3; Rare:83 | ||||
chr1:43946632-43946983 | Rare:94 |