Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179293658-179293918 | Common:3; Rare:79 | ||||
chr1:179365649-179365960 | Common:8; Rare:77 | ||||
chr1:179877760-179878014 | Rare:48 | ||||
chr1:179882151-179882879 | Common:1; Rare:260; Clinvar:8; Clinvar (benign):2 | ||||
chr1:179882926-179882950 | Common:1; Rare:13; Clinvar (benign):2 | ||||
chr1:179883007-179883040 | Common:3; Rare:11 | ||||
chr1:182839247-182839435 | Common:1; Rare:79 | ||||
chr1:182839556-182839792 | Common:2; Rare:104 | ||||
chr1:183185894-183185982 | Rare:12 | ||||
chr1:183186045-183186426 | Common:6; Rare:102; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr1:183472255-183472519 | Common:2; Rare:93 | ||||
chr1:183635629-183636123 | Common:5; Rare:142 | ||||
chr1:184051601-184051776 | Common:3; Rare:66 | ||||
chr1:184974343-184974859 | Common:2; Rare:117 | ||||
chr1:185156909-185157303 | Common:2; Rare:112 |