Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230604866-230604975 | Common:1; Rare:17 | ||||
chr1:232951420-232951730 | Rare:43 | ||||
chr1:234531149-234531352 | Common:1; Rare:34 | ||||
chr1:234600043-234600304 | Common:7; Rare:109 | ||||
chr1:234610145-234610338 | Common:2; Rare:87 | ||||
chr1:234610870-234611029 | Common:1; Rare:49 | ||||
chr1:234717795-234717973 | Rare:34 | ||||
chr1:234959778-234960033 | Common:1; Rare:49 | ||||
chr1:234962125-234962261 | Common:1; Rare:29 | ||||
chr1:235079668-235079907 | Common:1; Rare:44 | ||||
chr1:239730430-239730502 | Rare:10 | ||||
chr1:244450958-244451248 | Common:2; Rare:68 | ||||
chr1:244863706-244863857 | Rare:47; Clinvar:1; Clinvar (benign):2 | ||||
chr1:244970970-244971245 | Rare:75 | ||||
chr1:246569673-246569911 | Common:1; Rare:43 |