Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155934323-155934552 | Common:1; Rare:91 | ||||
chr1:155978369-155978619 | Rare:75 | ||||
chr1:156042759-156043032 | Common:1; Rare:49 | ||||
chr1:156053756-156053922 | Rare:43 | ||||
chr1:156054660-156055118 | Common:4; Rare:119 | ||||
chr1:156061078-156061304 | Rare:51 | ||||
chr1:156082463-156082576 | Rare:29 | ||||
chr1:156134779-156135309 | Common:3; Rare:131; Clinvar:23; Clinvar (benign):17; Clinvar (pathogenic):13 | ||||
chr1:156153269-156153623 | Common:2; Rare:67; Clinvar:1 | ||||
chr1:156193817-156194136 | Common:3; Rare:78 | ||||
chr1:156212875-156213031 | Common:1; Rare:40 | ||||
chr1:156282450-156282621 | Common:1; Rare:43 | ||||
chr1:156282789-156283039 | Common:2; Rare:57 | ||||
chr1:156284194-156284402 | Rare:50 | ||||
chr1:156338141-156338596 | Common:3; Rare:163 |