Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:231337830-231338049 | Common:2; Rare:81 | ||||
chr1:231528504-231528752 | Common:2; Rare:85 | ||||
chr1:232950479-232950658 | Common:3; Rare:63 | ||||
chr1:233613918-233614162 | Common:5; Rare:70 | ||||
chr1:234373347-234373582 | Common:1; Rare:115; Clinvar (benign):4 | ||||
chr1:234373656-234373792 | Rare:46; Clinvar (benign):2 | ||||
chr1:234608057-234608351 | Common:1; Rare:94 | ||||
chr1:235128764-235129043 | Rare:112 | ||||
chr1:235328151-235328356 | Common:2; Rare:63 | ||||
chr1:235866869-235867178 | Common:3; Rare:99 | ||||
chr1:236065083-236065381 | Common:3; Rare:114 | ||||
chr1:236604469-236604631 | Common:4; Rare:47 | ||||
chr1:236795094-236795443 | Common:5; Rare:146; Clinvar:3 | ||||
chr1:241519674-241519961 | Common:2; Rare:94; Clinvar:11; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
chr1:241848121-241848255 | Common:1; Rare:24 |