Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:124800406-124800454 | Rare:16 | ||||
chr11:125164558-125164759 | Rare:37 | ||||
chr11:125592543-125592900 | Common:6; Rare:117 | ||||
chr11:125625864-125626003 | Rare:45 | ||||
chr11:125887468-125887727 | Common:2; Rare:79 | ||||
chr11:126211639-126211809 | Rare:77 | ||||
chr11:126268814-126269192 | Common:1; Rare:145; Clinvar:2; Clinvar (benign):2 | ||||
chr11:126303771-126304083 | Rare:108 | ||||
chr11:126355531-126355752 | Common:1; Rare:59 | ||||
chr11:130314417-130314485 | Rare:21 | ||||
chr11:131911375-131911460 | Common:1; Rare:39 | ||||
chr11:134253297-134253606 | Common:2; Rare:110; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr12:401436-401644 | Rare:58 | ||||
chr12:2004427-2004660 | Common:1; Rare:73 | ||||
chr12:2812534-2812714 | Common:1; Rare:46 |