Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169529252-169529652 | Common:5; Rare:110; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:169781488-169781655 | Rare:31 | ||||
chr1:171373396-171373559 | Rare:36 | ||||
chr1:171438440-171438780 | Common:3; Rare:61 | ||||
chr1:171645050-171645187 | Common:1; Rare:29 | ||||
chr1:171661328-171661728 | Common:2; Rare:97 | ||||
chr1:171916410-171916950 | Common:4; Rare:84 | ||||
chr1:172449910-172450420 | Common:5; Rare:93 | ||||
chr1:172476180-172476550 | Common:1; Rare:61 | ||||
chr1:172497104-172497698 | Common:5; Rare:178 | ||||
chr1:172654510-172654900 | Common:1; Rare:79 | ||||
chr1:172746343-172746576 | Common:1; Rare:35 | ||||
chr1:172838866-172838973 | Rare:20 | ||||
chr1:172871060-172871340 | Rare:46 | ||||
chr1:172871360-172871610 | Rare:43 |