Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:230869566-230869836 | Common:3; Rare:49 | ||||
chr1:231241110-231241362 | Common:2; Rare:123; Clinvar:4; Clinvar (benign):2 | ||||
chr1:231337830-231338049 | Common:2; Rare:81 | ||||
chr1:231528485-231528758 | Common:2; Rare:91 | ||||
chr1:232805261-232805425 | Common:2; Rare:95 | ||||
chr1:232950464-232950664 | Common:3; Rare:72 | ||||
chr1:233613462-233613685 | Common:1; Rare:56 | ||||
chr1:233613895-233614153 | Common:4; Rare:70 | ||||
chr1:234373395-234373554 | Common:1; Rare:81; Clinvar (benign):3 | ||||
chr1:234373636-234373775 | Rare:53; Clinvar (benign):3 | ||||
chr1:235128768-235129078 | Common:1; Rare:128 | ||||
chr1:235866876-235867125 | Common:3; Rare:73 | ||||
chr1:236065072-236065342 | Common:2; Rare:106; Clinvar (pathogenic):1 | ||||
chr1:236523889-236524034 | Common:2; Rare:39 | ||||
chr1:236604456-236604646 | Common:4; Rare:57 |