Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228165678-228165810 | Rare:34; Clinvar (benign):2 | ||||
chr1:228165939-228166147 | Common:2; Rare:116; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):5 | ||||
chr1:228212928-228213241 | Common:2; Rare:74 | ||||
chr1:228406740-228407196 | Common:5; Rare:92 | ||||
chr1:228457824-228458113 | Common:1; Rare:115 | ||||
chr1:228487101-228487436 | Common:3; Rare:98 | ||||
chr1:229270983-229271352 | Rare:117 | ||||
chr1:229342489-229342741 | Rare:86 | ||||
chr1:229508215-229508453 | Common:1; Rare:95 | ||||
chr1:229558803-229559040 | Common:1; Rare:66 | ||||
chr1:229625902-229626306 | Rare:143 | ||||
chr1:230978830-230979157 | Common:1; Rare:119 | ||||
chr1:231241079-231241381 | Common:2; Rare:144; Clinvar:5; Clinvar (benign):2 | ||||
chr1:231337751-231338056 | Common:3; Rare:120 | ||||
chr1:231528497-231528758 | Common:2; Rare:87 |