Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255041-243255450 | Common:1; Rare:97 | ||||
chr1:243255714-243256243 | Common:1; Rare:170; Clinvar:5; Clinvar (benign):1 | ||||
chr1:243851069-243851176 | Rare:37 | ||||
chr1:244051219-244051460 | Common:1; Rare:50 | ||||
chr1:244451844-244452243 | Common:1; Rare:131 | ||||
chr1:244835142-244835337 | Rare:80 | ||||
chr1:244835575-244835766 | Common:3; Rare:86; Clinvar:1; Clinvar (benign):6 | ||||
chr1:244862948-244863328 | Common:4; Rare:147 | ||||
chr1:244863616-244864206 | Common:1; Rare:200; Clinvar:8; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
chr1:244864273-244864607 | Rare:121 | ||||
chr1:244969637-244969843 | Rare:59 | ||||
chr1:244970031-244970439 | Common:5; Rare:182 | ||||
chr1:244970918-244971086 | Common:1; Rare:47 | ||||
chr1:245154831-245154990 | Rare:39 | ||||
chr1:246565973-246566647 | Common:4; Rare:227 |