Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228103311-228103491 | Common:1; Rare:60 | ||||
chr1:228109235-228109491 | Rare:86 | ||||
chr1:228457796-228458120 | Common:2; Rare:133 | ||||
chr1:229271027-229271303 | Rare:93 | ||||
chr1:229508275-229508453 | Common:1; Rare:73 | ||||
chr1:229625953-229626254 | Rare:97 | ||||
chr1:231241108-231241362 | Common:2; Rare:125; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337823-231338049 | Common:2; Rare:83 | ||||
chr1:231338177-231338306 | Rare:35 | ||||
chr1:231528482-231528747 | Common:2; Rare:89 | ||||
chr1:232950426-232950658 | Common:4; Rare:89 | ||||
chr1:234373351-234373554 | Common:1; Rare:105; Clinvar (benign):3 | ||||
chr1:234373628-234373775 | Rare:56; Clinvar (benign):3 | ||||
chr1:234608062-234608312 | Common:1; Rare:79 | ||||
chr1:235128794-235129025 | Rare:87 |