Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:228457617-228457659 | Rare:17 | ||||
chr1:228457847-228458113 | Common:1; Rare:94 | ||||
chr1:229271027-229271294 | Rare:91 | ||||
chr1:229625977-229626249 | Rare:86 | ||||
chr1:230978758-230979108 | Common:2; Rare:135 | ||||
chr1:231241135-231241362 | Common:2; Rare:106; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337738-231338056 | Common:3; Rare:121 | ||||
chr1:231528474-231528826 | Common:2; Rare:113 | ||||
chr1:233613916-233614141 | Common:2; Rare:56 | ||||
chr1:234373421-234373550 | Common:1; Rare:74; Clinvar (benign):3 | ||||
chr1:234608203-234608267 | Rare:23 | ||||
chr1:235328149-235328657 | Common:5; Rare:156 | ||||
chr1:235866858-235867107 | Common:3; Rare:77 | ||||
chr1:236795551-236795687 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):3 | ||||
chr1:243255045-243255130 | Rare:22 |