Tag | Content |
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EnhancerAtlas ID | HS182-11495 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr19:45714590-45715870 |
Target genes | |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH19I045211 | chr19 | 45715040 | 45716150 |
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Enhancer Sequence | CTAAAAATAC AAAAATTAGC TGGGTATGGT GGTGGTGGAG GGGGGGCACC TGTAATCCCA 60 GCTACTCAGG AGCCTGAGGC AGGAGAATAA ATTGCTTGAA CCTGGGAGGT GGAGGTTGCA 120 GTGAGCTGAG ATCGCGCCAT TGCACTCTAG CCTGGGCGAC AGAATGAGAC TCTGACTGAA 180 AAAAAAAAAA AAAAGAAAAT GTCATTTTCA GAGGGCAAAG TGAGGAAGGT GCACCCTCAG 240 GACATTCTTG CCTCAGCCTG GGGAAAGAGA GTTTAAGCAA TTCCCCCAGA AAGGCACAGG 300 AACCTCAGCC CAGAGAGGGG CAGCTTCCTG CCTCGGGTCA GGAAGCACAG CCTTGGGCTC 360 CGAGAGTCCC TCGTCTCTAC CTCCCCAAGT TCAAATGTGC ATGCGTGAAG TTCCAAACCC 420 AGCCCCAGTG CTAACCCCTG GCTGCCTCCT CTTTCTGACT TCTCAGGGAA AAAAAAAAAA 480 ACCACATACA CACAAAAAAT CCCACAAGTC AGGAAACATC CATCACGGGC TGTCCAGCCC 540 AGGCCGGAGG GGCAGGAGTC AGCAGGGAGG TGACCTCAAG GTCTCCGTGG GGACTAGGAT 600 CCGGCGGGGC TGGGGGTGAG AGGCTGGAAA TTTTCCCACC CCGAGACTTT CCTGCGTCAA 660 CCCAGGAGGG CGCCCTGGAT GCCGCCAGCC CTGCCCCCAA CCTCCTTCCT CTCCTGACAG 720 GGCAGCTTCC CGGCTAAGGA TGGATGGGGA GGGTGTGCCA AGATGGAGCC ACCAGGACCA 780 GGAATGGACA GGCACTTTGA GATTGACCAG ACGAGGGACC CTGGCTCAGA GTGGCGAAGG 840 CCTGGCCTCA GAGCCACACA GCCAGGAGGT GTACATGGGT TGGCGTCGCT CCCAGCACAT 900 GCAGCCTCCC TCTACCTCCA CTACCCTGCC CAGGAGCTGG AGCCCAGCCC GGCCTTGGGT 960 GTGTGAGAAG CCACTGGCCC GGGGCCCTGC TTCCCCGGTC CTTCCTCCCC ACAACACACT 1020 CAGGACTCAG CCCTTCCTTG TGTTAAATAG AAACCTCTTT ATTCTAAGTA TCGAACGTTC 1080 CTTAATACAT TGGATTGGGG CCAGACCTTG AGGTGAGGGA AAGGGGCGGG GGAGCTGGGA 1140 TATTTCTGTA GAGACTTCCA GAACGACACT CACCACTCTG GGCTATGGCA GGAGGGGAGG 1200 TGCTGGGAAC AGGCTTCATG GCCTTGGGAA AATGCTTTGT CTCTTTGGCC TCTGTTTCCC 1260 CCTACCTTTT TTTTTTTTTT 1280
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