Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:229625956-229626261 | Rare:99 | ||||
chr1:230978753-230979108 | Common:2; Rare:137 | ||||
chr1:231241104-231241390 | Common:2; Rare:140; Clinvar:5; Clinvar (benign):2 | ||||
chr1:231337762-231338056 | Common:3; Rare:113 | ||||
chr1:231528450-231528831 | Common:3; Rare:120 | ||||
chr1:233613988-233614186 | Common:5; Rare:72 | ||||
chr1:234373347-234373554 | Common:1; Rare:106; Clinvar (benign):3 | ||||
chr1:234373645-234373766 | Rare:48; Clinvar (benign):3 | ||||
chr1:234608177-234608351 | Rare:58 | ||||
chr1:234608457-234608799 | Common:3; Rare:164; Clinvar (benign):2 | ||||
chr1:235128604-235129029 | Rare:168 | ||||
chr1:235328151-235328648 | Common:4; Rare:154 | ||||
chr1:235866842-235867132 | Common:3; Rare:83 | ||||
chr1:236281936-236282069 | Common:2; Rare:35 | ||||
chr1:236523897-236524060 | Common:2; Rare:44 |