Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:43206821-43207194 | Common:2; Rare:184 | ||||
chr1:43348300-43348800 | Common:4; Rare:121 | ||||
chr1:43348835-43349276 | Common:6; Rare:344; Clinvar:10; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:43349330-43349720 | Common:1; Rare:166; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr1:43381707-43381834 | Rare:16 | ||||
chr1:43523110-43523370 | Rare:50 | ||||
chr1:43531516-43531916 | Common:4; Rare:216 | ||||
chr1:43532089-43532495 | Common:3; Rare:109 | ||||
chr1:43536160-43536470 | Common:3; Rare:144 | ||||
chr1:43536540-43536855 | Common:2; Rare:101 | ||||
chr1:43549948-43550536 | Common:16; Rare:295 | ||||
chr1:43552106-43553287 | Common:11; Rare:348 | ||||
chr1:43594080-43594630 | Common:7; Rare:85 | ||||
chr1:43684591-43685019 | Rare:207 | ||||
chr1:43763737-43764137 | Common:3; Rare:97 |