Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:126063280-126063442 | Common:3; Rare:34; Clinvar (benign):1 | ||||
chr11:126211271-126211456 | Common:1; Rare:50 | ||||
chr11:126211564-126211830 | Rare:127 | ||||
chr11:126266474-126266787 | Rare:97 | ||||
chr11:126268517-126268646 | Common:2; Rare:32 | ||||
chr11:126268769-126269234 | Common:2; Rare:188; Clinvar:3; Clinvar (benign):7 | ||||
chr11:126269323-126269432 | Common:1; Rare:40 | ||||
chr11:126303952-126304116 | Rare:99 | ||||
chr11:126304231-126304336 | Common:1; Rare:46 | ||||
chr11:126355518-126355778 | Common:2; Rare:75 | ||||
chr11:129279476-129279712 | Common:2; Rare:94 | ||||
chr11:129895434-129895687 | Common:2; Rare:92 | ||||
chr11:130002452-130002720 | Rare:60 | ||||
chr11:130002749-130002927 | Common:2; Rare:34 | ||||
chr11:130069653-130070071 | Common:2; Rare:146 |