Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:6625046-6625234 | Rare:74 | ||||
chr1:6625642-6625692 | Rare:9 | ||||
chr1:6701466-6701635 | Rare:48 | ||||
chr1:6701747-6702059 | Rare:94 | ||||
chr1:6784458-6784841 | Common:1; Rare:122 | ||||
chr1:6784929-6785346 | Common:1; Rare:129 | ||||
chr1:6785441-6785557 | Common:2; Rare:42 | ||||
chr1:6785751-6785953 | Common:1; Rare:47 | ||||
chr1:7771104-7771388 | Common:4; Rare:116 | ||||
chr1:7771542-7771706 | Rare:31 | ||||
chr1:7783998-7784034 | Common:1; Rare:12 | ||||
chr1:7784127-7784188 | Rare:26 | ||||
chr1:7940763-7941038 | Rare:48 | ||||
chr1:7953945-7954465 | Common:5; Rare:149 | ||||
chr1:7961300-7961785 | Common:4; Rare:156; Clinvar:2; Clinvar (benign):3 |