Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:67429989-67430467 | Rare:181 | ||||
chr1:70205484-70205770 | Rare:107 | ||||
chr1:70221303-70221543 | Rare:106 | ||||
chr1:70354648-70354895 | Rare:77 | ||||
chr1:70411027-70411285 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):1 | ||||
chr1:71080945-71081379 | Rare:114 | ||||
chr1:74198091-74198340 | Common:3; Rare:131 | ||||
chr1:74732994-74733320 | Common:6; Rare:112 | ||||
chr1:75724277-75724598 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):3 | ||||
chr1:77219398-77219536 | Rare:59 | ||||
chr1:77682641-77682716 | Rare:19 | ||||
chr1:77683328-77683628 | Common:1; Rare:93 | ||||
chr1:77888270-77888730 | Common:3; Rare:101; Clinvar:2 | ||||
chr1:77979008-77979334 | Common:3; Rare:110 | ||||
chr1:78004546-78004960 | Common:4; Rare:97 |