Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228109235-228109468 | Rare:80 | ||||
chr1:228140284-228140363 | Common:1; Rare:40 | ||||
chr1:228457830-228458118 | Common:1; Rare:111 | ||||
chr1:229271011-229271341 | Rare:107 | ||||
chr1:229508269-229508445 | Common:1; Rare:70 | ||||
chr1:229625883-229626269 | Rare:123 | ||||
chr1:231241108-231241272 | Rare:91; Clinvar:3 | ||||
chr1:231337830-231338056 | Common:2; Rare:82 | ||||
chr1:231528579-231528747 | Common:2; Rare:61 | ||||
chr1:232950280-232950664 | Common:5; Rare:117 | ||||
chr1:234373351-234373554 | Common:1; Rare:105; Clinvar (benign):3 | ||||
chr1:234373642-234373775 | Rare:51; Clinvar (benign):3 | ||||
chr1:234608057-234608356 | Common:1; Rare:97 | ||||
chr1:235128652-235129032 | Rare:154 | ||||
chr1:235328151-235328579 | Common:3; Rare:122 |