Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155209112-155209250 | Rare:63 | ||||
chr1:155254903-155255252 | Common:3; Rare:77 | ||||
chr1:155308650-155308978 | Rare:71 | ||||
chr1:155324162-155324578 | Common:3; Rare:153 | ||||
chr1:155688648-155688773 | Common:1; Rare:42 | ||||
chr1:155859359-155859590 | Common:2; Rare:55 | ||||
chr1:155978475-155978632 | Rare:39 | ||||
chr1:156054611-156054872 | Common:3; Rare:73 | ||||
chr1:156136015-156136336 | Common:3; Rare:100; Clinvar:14; Clinvar (benign):14; Clinvar (pathogenic):8 | ||||
chr1:156193828-156194132 | Common:3; Rare:78 | ||||
chr1:156282787-156282935 | Common:1; Rare:41 | ||||
chr1:156728385-156728482 | Common:1; Rare:18 | ||||
chr1:156751343-156751816 | Common:1; Rare:116 | ||||
chr1:156767386-156767735 | Common:2; Rare:96 | ||||
chr1:157138346-157138450 | Common:2; Rare:23 |