Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36464247-36464486 | Common:2; Rare:67 | ||||
chr1:37474391-37474581 | Common:1; Rare:77 | ||||
chr1:37595888-37596075 | Common:2; Rare:62 | ||||
chr1:37859550-37859780 | Common:3; Rare:75 | ||||
chr1:37989969-37990220 | Common:1; Rare:83 | ||||
chr1:38859673-38859951 | Rare:114 | ||||
chr1:38873333-38873554 | Common:3; Rare:70 | ||||
chr1:39026225-39026397 | Common:1; Rare:45 | ||||
chr1:39081236-39081458 | Common:1; Rare:47 | ||||
chr1:39738691-39738907 | Common:2; Rare:48 | ||||
chr1:39883447-39883570 | Common:1; Rare:51; Clinvar (pathogenic):1 | ||||
chr1:40040444-40040801 | Common:3; Rare:108 | ||||
chr1:40161252-40161405 | Rare:39 | ||||
chr1:40257908-40258265 | Common:4; Rare:96; Clinvar:7 | ||||
chr1:40449958-40450159 | Common:4; Rare:79 |