Tag | Content |
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EnhancerAtlas ID | HS182-14644 |
Organism | Homo sapiens |
Tissue/cell | Spleen |
Coordinate | chr21:47308920-47310440 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF4 | MA0039.3 | chr21:47310113-47310124 | CCACACCCTGC | + | 6.62 | Klf1 | MA0493.1 | chr21:47310111-47310122 | GGCCACACCCT | + | 6.32 | ZNF263 | MA0528.1 | chr21:47309436-47309457 | CACCCCTTCCTCCCCTCCTCA | - | 6.28 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr21 | 47309847 | 47309949 | chr21 | 47309974 | 47310228 |
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| Number: 1 | ID | Chromosome | Start | End |
GH21I045889 | chr21 | 47309215 | 47310523 |
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Enhancer Sequence | CCTAAATACA CCTTTATGGG CTCAATACCA CTTTGCCATA AGCAAGTAAG TAAAGAAAGG 60 AATCTTTCGT TCTGGCCCGT GCACTGTTGC ATGACTGGAG CTGTGTTGAT GCCCTCATCC 120 TGGGTCTGTT TCGTCTGTGG AGACAAAGAG CGATGTGTGT GGGAGTGGGG GTTCAGGCAG 180 GAGCGCTCAC AGGGGCTTCA GAGACGGTGG AGTGGAGAGA GGAGCTGTTA AATGTAAGTG 240 CCCCGAGCTG CCGTCAGCAG CTGCATGCGG GCCAGCAGCC TCTGATTTGC CTTCCTCCGA 300 CTGCAAAAGT CGTTAAATCA CATCAAGCCT GGGGCCTGCT TAGAAGCTGT CAGGACCGTC 360 TTCTCTACTG TTCCCCTGAT GCCTCCATTG TGAAGACCCA GCCCAGCTCT GAATGCAGGG 420 ACAGCACCTG TGCTTCCTGG CAGATGCAGC TCAGAGCAGG AAACCTGGTC TCCACCTTGG 480 GCAGACAGCA ACGGTGCAGG CAGTGTGGTT GCCTGGCACC CCTTCCTCCC CTCCTCATGG 540 CCAGGGCCAC GGCCAGCCTC CTCCTCCCTT CTTCTGCAGC CCGCCCTTGG GAAAGGATGC 600 TGTGGAGTTA GAGGCGGGGA GCTTCAGGCC TGGCTGCGTC TTTCCCTAGC TTGGGGACCT 660 TTGAACAATT CCTGAGTCTC CCTGCCATGG CTCTTGTGGC AGTACATTGC GGTGGCTACA 720 GATGTTTGTT GCCGTGAGTG CTGCTCAGCC CTCACGTGCT TGTCCATCTG CCTGTGGCAC 780 TGGCATCCAG GGAACAGCTT TCAAGTACAT GGAGATTTCA CCTGCAGCTT CTGATCCCCC 840 CAGATTCTCT CCAGTGTGAC TTTAAGGAAA AGATACTTAT GAAAACCAAA GGGAGCTTTT 900 AGAAGTCAGC GTAGCTCCGA GACGGAGGCC TGTTTCTGCT CTGTCTTGGA GCTGACAGTG 960 GCTCCAGCCA ATGACCCCAT TCCTCCAGTA GCCCTCAGTA AGGAGTGCTG TGTCCCTGAC 1020 CTCAGTACTT GGCCCATGCC AGGGGCTGGG ACTGCGTCTG TCACTGCCAG GGTGGGAGAC 1080 GTGGCCTCGC AGCTGTCTAA GGGGCAGTTT CCAGCAGCTA CTCTGCTGCG GGAGAGAATG 1140 GAGCAGACAG GTCATGAGGC CAGCATGAGA GCATGGGGAG GGGTTCTGCC TGGCCACACC 1200 CTGCAACTAG ACAACACTGC ACGCCCGCTG GGCAGCACAG AAAAGGCTGA ACAGACCAGC 1260 TGTTGGCGGG GCCGTGGAGG AGCTGCAGCT CTGTGCGCAG CTGAGGGAAA TGTGGATAAC 1320 AGAACCTGGA ACTCGGTGCA CTTAGGGGGA TGTGGATAAT ACAACCTGAA ACCCTGCGCT 1380 GCTGAGGGGA ATGTAGATAA TAGAACCTGG AACTCTGTGC ACTGCTCAGG GGAATGTGGA 1440 TAATAGAACC TGGAACTCTG CACAGCTGAG GGGAATGTAG ATAATAGAAC CTGGAACTCT 1500 GCACTGCTGA GGGGAATGTA 1520
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