Tag | Content |
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EnhancerAtlas ID | HS182-03755 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr11:57328890-57330440 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
BCL6 | MA0463.2 | chr11:57330318-57330334 | AATACCTCGAAAGCCT | - | 6.07 | Stat6 | MA0520.1 | chr11:57329372-57329387 | ATTTCTCTGGAACAA | - | 6.37 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 57329358 | 57329460 | chr11 | 57329966 | 57330435 |
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Enhancer Sequence | ATTTCAATAG AGTAATGGAC GAAACATGGA TGTGATTATG TGAATGTGTA TGGATATACG 60 GTAAGGAAGG AGATGAGAGG GGAGAAGGAA GGTTTCACAG AGGGTGCACT CTGTGAGCTG 120 GGCCATGCAG AATGAACAGG AATCCATAAA GCAGAGAAGG GGAGAAGCAC CAGGGCAGAG 180 GGCCCAGATG GGAAACATAA GTACAGTATG TCCTGCAGAA GGTTAATAGG TAGTACAGGA 240 AAAGGGTTCC AAGGTCAAGT ACATTTGGTA AATCTCGGCT AAAGAGGTTT CTTCACTGGA 300 GAACTTCCCA CAGCCTTTAA TATGCTATTG TGTATGGTGA TTGACCAAGC TGTGGGCCCA 360 CAGCATGCAG TACTTCTCAA ATGTATTTGA CAAAGGAATG CTGCCCCTCT TTTAGAGTCC 420 ATCTTGTGGG ACTACAGGCC TTTTCTTGTT GGGGAAGATA AAGACACTCA AGGGCAGGTC 480 ACATTTCTCT GGAACAATGA ATTGGTACAA ACCAGTGGTT CTCAACCAGG GGCGATTTTA 540 CCCAGCCAGG GACATTCGGT AATATCTGGG AACATTGTTC CGTTGTCATA AATCGGGAGA 600 GTGGATAGAG GCCAGAGATG CTGATAAACA TCCTAACAAA GAATTATCTG GCCGAACAAG 660 AGGGGAGACC GCTGCCCTGC AGGGTGAGTC TCAGGCCTGG TCACATTCAC CACAAGCTGA 720 CTGAAGGGCC TTTGGGCCTT AGGCGAACAT CAGCAGTAGT ACCCTGGCAG TACTCCTCAT 780 AGACCCGTGG TGGTGGTGGA CAAGGGGAGA GACTCCTATA TCTGGGGAAA AGGGAGGGAA 840 GAGTGGGAAG GACTGTGTCC TGTGGTTTCA GTGCCAGCTT AGCTGCAGTA GCACAGAGCA 900 CTAGAGAGAT TTCTAAGGTT TCCGACTCCA GGCCCTGGCC CATGGACAGC AACTGTGGAC 960 CTCTCTGGGG CCCAGCAGTG AACTAACCAC CCTAAGGGGA AGAACACAAG CCTGGCTGGC 1020 TTCACCACCT GCTGATTGCA GAGCCCTAGG GCCTTGAGCG AACGTAGGGC ATAGCCAGGT 1080 AGTGATTACA GCGGGCCTTG AGCAAAACCC AGTCTTGTGC TGGCTTCAGG CCTGACCCAG 1140 TGCAGTCCCA ATTCTGGTGA CCATGGGGAT GCTTGTGTCA CACCTCACCC AGCTCCAGGG 1200 AGCTCAGCAC GGAGAGTAAG ACTCCATTTG TTTGGGAGAA AGTAAGGGAA GAAAATGAGA 1260 GTCTCTACCT GGTAATCCAG AGAATTCTTC CTGATGTTAT CCAAAACCAC AAAGGTAGTA 1320 ACCTCTAAAA GTCTGCAAGA ACTACAGTGT TACTAGGCTT GGAGTGCCCC CTTATGTAGA 1380 CATGGCTGCA GTGACCAAAA CTTAGATCAC AACAGCCAAG CCCCTTCCAA TACCTCGAAA 1440 GCCTTCCCAA GAAGGATGAG TACAAACAAG CCCAGACTAC AAAGACTATA ATAAATACCT 1500 AACTCCTTAG TGCCCAGACA CCAACAAACA TCCACAAGCT TCAAGACGAT 1550
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