Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230978904-230979127 | Rare:85 | ||||
chr1:231241110-231241362 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337830-231338049 | Common:2; Rare:81 | ||||
chr1:231528482-231528738 | Common:2; Rare:86 | ||||
chr1:232805328-232805446 | Common:1; Rare:66 | ||||
chr1:232950476-232950664 | Common:3; Rare:66 | ||||
chr1:234373311-234373592 | Common:1; Rare:135; Clinvar (benign):4 | ||||
chr1:234373617-234373775 | Rare:64; Clinvar (benign):3 | ||||
chr1:234608029-234608283 | Common:1; Rare:81 | ||||
chr1:235128788-235128951 | Rare:61 | ||||
chr1:235328109-235328425 | Common:2; Rare:90 | ||||
chr1:235866852-235867238 | Common:3; Rare:125 | ||||
chr1:236065047-236065344 | Common:2; Rare:114; Clinvar (pathogenic):1 | ||||
chr1:236523616-236524060 | Common:5; Rare:106 | ||||
chr1:236540491-236540666 | Common:3; Rare:64 |