Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:154432737-154432961 | Common:1; Rare:41 | ||||
chr1:155008724-155008969 | Rare:61 | ||||
chr1:155178808-155178993 | Rare:53 | ||||
chr1:155441277-155441582 | Common:7; Rare:65 | ||||
chr1:155904480-155904772 | Common:2; Rare:84; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr1:155965074-155965645 | Common:3; Rare:127 | ||||
chr1:156745286-156745583 | Rare:65 | ||||
chr1:158177903-158178047 | Common:2; Rare:33 | ||||
chr1:158181100-158181368 | Rare:72 | ||||
chr1:158283824-158284165 | Common:1; Rare:69 | ||||
chr1:158833362-158833480 | Common:1; Rare:26 | ||||
chr1:160681455-160681478 | Rare:6 | ||||
chr1:160841419-160841680 | Rare:58 | ||||
chr1:161214370-161214617 | Rare:55; Clinvar:1 | ||||
chr1:161216944-161217273 | Rare:52 |