Tag | Content |
---|
EnhancerAtlas ID | HS095-05929 | Organism | Homo sapiens | Tissue/cell | HMEC | Coordinate | chr11:94370970-94373400 | TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6B | MA0731.1 | chr11:94371217-94371234 | TGAATTCTTCAAAAGCA | - | 6.35 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| | Number: 1 | ID | Chromosome | Start | End |
GH11I094637 | chr11 | 94370871 | 94373747 |
| Enhancer Sequence | GGCTTGAAGC CTTGTTGGGG AGAGAGACAC AGGAGCACAA AGTACCAATG TCATGTGGAA 60 AGTGAGCAGA GAGTGGTAGA GCACAGCCGT CGGACTGGGA GGATTCCCAA GCTGAGTCTG 120 GAAGGAGCTG CATGCCTAGT CATTCCTTCT ATGATCTAAT AATGCTTTGC CCATTCCCCT 180 CTGCAACACC TAACACTGTG ATGTATTTTA ACCATCAGTT TACACATACT TCTCTCCTGT 240 GAGACTGTGA ATTCTTCAAA AGCAGGTACT GTGTTTAATG AAGTGTGCCC AGGACTTTGC 300 TCAGTGACTG GATGACACAG TAGGAGTAAC AAGAAAGTTC ACATGGGTGA ACCGTGGTAG 360 GTGGACATCG TCTCTCTCAC CTCTTCCCAA ATCAAGGATG AAGTACATCT TCATAAATCC 420 TCATGTGAAT TATTTTGCTA CCTCTAGAAG CATTTTCTAA AACAAGGTGC AGCAATCAGT 480 TGAGTGAATT TGTCACCAGA GCTTATGTTT TCTGAAAGAA CCCTATCCTC AGGCAGTTGT 540 TCCTAAGAGG TGAGTTGTGG ATTTAGTTCA CATACCTTCC TTCGTGGCTT AAAATGCTCC 600 ACATGCCTGT CTCCCCAACA GCATCAGATC ACCATGCAGT AAAATACCAA GTCAGAACAG 660 CCAATGCTGA AAAGAGTGAC AGTTTCCTTT CATGATGCAA TGCACTTGGA GCCAGGGGAC 720 AGGGAGACAA TAACTGCAAG GAGAAGTGAT GACAACCCTA CTTTAATATA GTAGTTCCTT 780 TTGAATTTTA TAGACTTACC CGTTAATCTC TAGAATTTTG AAAAAATTCC TTAAGTGATG 840 TGAGCAAATA ACACTTTGCC TTGGGTTAGC CTTTTCCTTT CCCTTGAAGA TTCCACAAAT 900 ATGTCAGCGC TGGAAATGAT CCTTTGGCTT TGAACTATGT GAAGACTGCA GAAGGACTGG 960 TTGGTAAGCA CCCACATCCT GGGGTGAGAA TCACATCCAG TTTATACCTC CCTGTGCACA 1020 CTTGTATAAA ACAACTATAA GACACACGAG AGATCTGGAA GCCAGTTCCT CATAAGTAAG 1080 AATTGGTAAG AGCTCTTAAG CAGCATGTCT GAGGTTTAAT AACTCGCCCT GTCTGGAGCC 1140 TTTTGTGTGT CTCACTTTCT TCTTAGCAAA ACATGAGCAT TACACTCTGT GCTGGAAGAT 1200 TCCCTTCCTT CTTCCGGGCT TTTGATTACC CAATCCTTCT TTACTTTCAC TTCTTGCTCA 1260 AAGCAGCTCT TTCTCAGCCA TTTCTAAAAA AGGTTTATGA GATGCTGCAG GGCTGTGTCT 1320 CTAAATTGGG CCCTGTGTGC CTATATCCTC ATTCTCTGCA GCTGCTGAAT TCTTTCTGTG 1380 GGATCAGCCT TCTTCTAAGT GCTGGGGTGA TGGGAACATA GCTGTAAACT GATTTTGACA 1440 GGAAGCATCA CTTCCGGCTG GAAACAAGTC CCTGGTTTAT GCAGCACATA GTACTAACTG 1500 TGGAACACTG TTAAACATGT CTCATTCCGC CCCCTCCACC AGCAAAAGGC CTTGCTGCTC 1560 AGTTGTGCAC CAGATGATGT GGCATATGCA CATACTGGCC ACTAATGACA AAGCCTGACA 1620 CCATGCAGTG GACATCTCTT GGGACCTCAG CCTCTTTCTC CTGGAACTGA CCCCATCCTC 1680 CCTTCGCTAC ATGATCACCA TGGGTGGATT CCCAGCAGCC ATGCTTGTAA CATGCATCCT 1740 GTCCTCTCTG GCCACAGACA ACTACAATAC AGATGAGCAG CCCACCCAAG ATTCCTTCTC 1800 TAAGAATTTA GAACTGGGAA TGGAGGAGAG AAAGAGAGAG ATACTGATTC TACCAGAGAC 1860 AATGGGATGA GATAGCATGG TTGTTGGAAC CATGGCTGGA ACTGTAAAGC ACAAATTGGA 1920 CAGCAGATAA AGTTGGTTCA CAGAGAGAGA GAGAATGATG AAGCCATAGG GATCCAAGTT 1980 TCCCTATGGC TTTCCTCACC CTAACTCCTG TCCTTCCACA GGTCAGGCTG CATTTGTATC 2040 CTGGGTCCAC AAGACATCGT TTCCTTAAAA CCAATCCCCC TGATTTTGCT AAGGTGAGTC 2100 GGAACAAGTT GATTTCTGTT ACACACACAA ACACACACCC CACATGAGAC AGCCAGGTAG 2160 GAAGTGCTCC CTGGCAGAGC CTCCCTGACC TGCACACTGG GAGGAATGCA CGCTGGGGTG 2220 GAGCCTTGGG AGGTTCGCGT GGTTTGCAGT GGGGAGGAGC CTGCCGCCCT CTTCCTGGGT 2280 GGAACCTGGG ATTCAGTTCG CCAGGCAGGA AGTGCAGTAG CAGGACTCTG GCTTTCCGGA 2340 GAGTCTCTGT TTTTCCTTTT TTTTTTTCCC TTTTCGCCCA ATAAATACCA TTTTTCTCAC 2400 CCTTCAAAGT GTCTGCAAGC CTAATATTTC 2430
|
| |
|
|
|