Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:40979359-40979797 | Common:5; Rare:137 | ||||
chr1:42335157-42335362 | Common:4; Rare:105 | ||||
chr1:42455998-42456114 | Rare:37 | ||||
chr1:42456387-42456583 | Rare:70 | ||||
chr1:42658275-42658495 | Common:2; Rare:65 | ||||
chr1:42682158-42682432 | Common:2; Rare:70 | ||||
chr1:42766967-42767317 | Common:5; Rare:120; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:42817004-42817136 | Common:1; Rare:32 | ||||
chr1:42846392-42846638 | Common:1; Rare:68 | ||||
chr1:42958694-42959101 | Common:4; Rare:103; Clinvar:6; Clinvar (benign):5 | ||||
chr1:43172164-43172353 | Common:3; Rare:80 | ||||
chr1:43358667-43359006 | Common:7; Rare:106 | ||||
chr1:43367961-43368190 | Rare:60 | ||||
chr1:43389757-43389966 | Common:4; Rare:93; Clinvar:1 | ||||
chr1:44674421-44674749 | Common:3; Rare:85 |