Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155934335-155934486 | Common:1; Rare:69 | ||||
chr1:156054625-156054877 | Common:3; Rare:70 | ||||
chr1:156134951-156135241 | Common:3; Rare:61; Clinvar:6; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:156135969-156136418 | Common:4; Rare:144; Clinvar:28; Clinvar (benign):20; Clinvar (pathogenic):11 | ||||
chr1:156193832-156194118 | Common:3; Rare:75 | ||||
chr1:156282797-156282924 | Common:1; Rare:35 | ||||
chr1:156293174-156293374 | Common:1; Rare:55 | ||||
chr1:156338152-156338551 | Common:2; Rare:146 | ||||
chr1:156641870-156642180 | Rare:68 | ||||
chr1:156728394-156728630 | Common:2; Rare:66 | ||||
chr1:156767374-156767588 | Common:1; Rare:72 | ||||
chr1:157045107-157045441 | Common:2; Rare:54 | ||||
chr1:157138342-157138424 | Common:1; Rare:19 | ||||
chr1:158999873-159000003 | Rare:32 | ||||
chr1:159015568-159015811 | Rare:45 |