Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:24746084-24746484 | Rare:117 | ||||
chr1:25032200-25032640 | Common:2; Rare:75 | ||||
chr1:25233114-25233514 | Common:2; Rare:148 | ||||
chr1:25239721-25240203 | Common:9; Rare:362 | ||||
chr1:25544284-25544749 | Rare:186 | ||||
chr1:25544821-25545221 | Common:10; Rare:139 | ||||
chr1:25616324-25616914 | Common:22; Rare:405 | ||||
chr1:25766705-25767105 | Common:4; Rare:173 | ||||
chr1:25773572-25773819 | Common:1; Rare:45 | ||||
chr1:25800757-25801219 | Common:2; Rare:186; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr1:25874920-25875310 | Common:2; Rare:113 | ||||
chr1:25875370-25876240 | Common:8; Rare:445 | ||||
chr1:25878708-25879108 | Common:2; Rare:97 | ||||
chr1:25890250-25890580 | Common:2; Rare:57 | ||||
chr1:25890600-25890860 | Common:5; Rare:137 |