Tag | Content |
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EnhancerAtlas ID | HS076-37653 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr22:22080390-22081580 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
KLF16 | MA0741.1 | chr22:22081335-22081346 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr22:22081335-22081345 | GCCCCGCCCC | + | 6.02 |
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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 |
GH22I021726 | chr22 | 22081001 | 22081210 |
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Enhancer Sequence | GCCGTGGGGT GCGGGCAGCT GCAGATTCAC CTCACCCAGA CCCACATGTC CCCAGGGTCT 60 AGGACCATGG TCCCCAAAGA GCAGTGCACA AGCCAGGGCC CTGCCAGCGC TGTCCAGGAA 120 GGACCAGCCG CAGCCTGCTG TGGCCCCAAG CTGGTCCCAG AAGGTTCCAG GAAGGAATCT 180 CATCTATTCA GGCGCAAGGC CCCCAGAATG ACAAGAATGT TGCCAAAGAC AGGCGTTTGC 240 CCTTTACATC ATGCATCTGC ACCTTAGGGT CGGCAAATTC TCAGGCCGTT GAATTCTCAC 300 AACATCCTGA GAAATAGGCA TCCCTGCCCG CTAGCGGCCA CCACAGTCCC ACAGGCGGGT 360 ACTCAATCCA GAGCACAGGT GCTCTCCGCT CTCGGTCCCA CCTGGCCTGA GAGGGAGGAG 420 CATCAGCGGA GGACAGTCCA GTCCCCAGGA GGGAGGGGAC CCTCTGACCA CCAGTGTTCC 480 AGGCAGGAGG AAGCGGTGCG TCCCCATCAG GGTCCTGTGT TACCCCAGGG TCCTCCATGC 540 TGTAACTGTT CTCTATTTGC TCAAAGCCTG TAACTCTCAG TGGAGATACC ACCCCTGGTG 600 GCTGTAGCCC AGCCTGCTGC CCTCCCTTGC TGGCCCCTTC CTGCACCTGG GCTGTCCCCA 660 CAGCAAGTGC CACTGGCTGA GCCTCCCAGC TGTGAGGCAG ACAGATGCAG CGACAAGCTC 720 AGATCTCAGC TCTCGCCTCC ACCTTGTGGT TTCTCTGAGT GTCACACATC CCCAGTGGGA 780 TGCAGAGGAC GCTACTAACT CTTCCTGGAC CAGAGTGCCT AGGGCTCTGC AGAGTAAACA 840 CTGAGGGCAC CGCTAATTAC AAAAAGCCTT GTTTCCAACC AAAACAGGCT TGCTGTTTCC 900 CAAGCACACT TCGCATGGGC TTTATTTGGA GACCTTCATT ATACAGCCCC GCCCCCAAGG 960 CAATCTTACC TGAAGAGCCT GCTGCCCTGG GTCCCAAATG TCCCCCAAGT CCCTGTCCCT 1020 GTCTCCTGCC TTGAGTCTGG TCACTGCACA GATGCCTCCC GTGCGCTTCA TGTGGTCTCA 1080 GTCCTGATGG CAACCCTTGT CACTAGCCCT CAAAGGGGTC CTGGCAGTAG TGGCCAGGGC 1140 TGTATTTGTG GTCACTGAGA GGCATGTCAT GTTAAGTTTT AACTTGGCTT 1190
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