Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:234373388-234373578 | Common:1; Rare:94; Clinvar (benign):4 | ||||
chr1:234373645-234373776 | Rare:49; Clinvar (benign):3 | ||||
chr1:234608071-234608281 | Common:1; Rare:67 | ||||
chr1:235328080-235328657 | Common:5; Rare:176 | ||||
chr1:235504412-235504699 | Common:4; Rare:83 | ||||
chr1:236064955-236065367 | Common:4; Rare:145; Clinvar (pathogenic):1 | ||||
chr1:236281925-236282249 | Common:6; Rare:95 | ||||
chr1:236523894-236524036 | Common:2; Rare:40 | ||||
chr1:236604451-236604645 | Common:4; Rare:61 | ||||
chr1:236794995-236795336 | Common:5; Rare:118; Clinvar:2 | ||||
chr1:236795552-236795687 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
chr1:239386483-239386691 | Rare:32 | ||||
chr1:243255176-243255365 | Common:1; Rare:39 | ||||
chr1:243255752-243256113 | Rare:99; Clinvar:4 | ||||
chr1:244451708-244451944 | Rare:76 |