Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:224330115-224330456 | Common:7; Rare:112 | ||||
chr1:224434815-224434945 | Rare:30 | ||||
chr1:225427971-225428329 | Common:3; Rare:127; Clinvar:4; Clinvar (benign):3 | ||||
chr1:225777716-225777960 | Common:3; Rare:86 | ||||
chr1:225924259-225924453 | Common:5; Rare:48 | ||||
chr1:225999316-225999618 | Common:2; Rare:101 | ||||
chr1:226062011-226062094 | Common:1; Rare:25 | ||||
chr1:226062426-226062860 | Common:1; Rare:153 | ||||
chr1:226407855-226407887 | Rare:10 | ||||
chr1:226870493-226870637 | Common:1; Rare:47; Clinvar (benign):1 | ||||
chr1:226939991-226940364 | Rare:132; Clinvar:3 | ||||
chr1:227735231-227735488 | Common:3; Rare:150 | ||||
chr1:228082487-228082765 | Common:3; Rare:115 | ||||
chr1:228103317-228103489 | Common:1; Rare:57 | ||||
chr1:228109235-228109468 | Rare:80 |