Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235503966-235504123 | Common:3; Rare:44 | ||||
chr1:235504125-235504308 | Rare:58; Clinvar:3; Clinvar (benign):5 | ||||
chr1:235649308-235649532 | Common:1; Rare:54 | ||||
chr1:235649988-235650078 | Rare:18 | ||||
chr1:235866530-235866708 | Common:1; Rare:39 | ||||
chr1:235866711-235867257 | Common:5; Rare:159 | ||||
chr1:236142331-236142591 | Common:4; Rare:62 | ||||
chr1:236142726-236142825 | Common:1; Rare:40 | ||||
chr1:236142843-236142947 | Rare:47 | ||||
chr1:236281495-236281694 | Common:2; Rare:60 | ||||
chr1:236281817-236282384 | Common:7; Rare:159 | ||||
chr1:236395847-236395947 | Common:1; Rare:24 | ||||
chr1:236523274-236523353 | Rare:19 | ||||
chr1:236523375-236523472 | Rare:15 | ||||
chr1:236523563-236523696 | Common:2; Rare:26 |