Tag | Content |
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EnhancerAtlas ID | HS026-27577 |
Organism | Homo sapiens |
Tissue/cell | CNCC |
Coordinate | chr5:141743320-141744690 |
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) |
KLF5 | MA0599.1 | chr5:141744253-141744263 | GCCCCGCCCC | + | 6.02 | MEF2A | MA0052.3 | chr5:141743823-141743835 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr5:141743823-141743835 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr5:141743822-141743837 | TTCTATTTTTAGTAG | - | 6.57 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_34287 | chr5:141741761-141746021 | HCT-116 |
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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 |
GH05I142355 | chr5 | 141735231 | 141745153 |
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Enhancer Sequence | TGTGTGTGCA TGTAGTCCTA GCTAATCAGG AAGCCGAGGC AGGAGGATGG CTTGAGCCAG 60 GGAGGTCATG GCTGCAGTGA ACTGTGATGC CACTGTACTC CAGCCTGGGC AACAGTGCGA 120 GACCCTGTCT TAAAAAAAAA AAAAGATATG TGCCAGGTAT TCAGCACCGT GCCTTGCACG 180 CAGCAAACCC TTATAACATT GGTTGTTATT TATGGAGAGG AAAAGGATAA AGGGGTGGGA 240 AGGCAAGAGA AGAGGGCTTA GGGTACTCTG CCCTCTAATG CTGGACCATT CAGATGAGGT 300 CCTGATGAAG CTCTGTCCAC CTGAAGCTTT TATTTTTATT TATTTATTTT GAGACAGGGT 360 CTCGCTCTGT CACCCAGGCT AGAGAGCAGT GGCATGATCT TGGCCCACTG CAACTTCCAC 420 CTCCCATGCT GAAGCGATTC TCCCACCTCG GCCTCCTAAG TAGCCGGGAC TACGGGCACG 480 CATCATCATG CCCAGCTAAT TTTTCTATTT TTAGTAGAGA CAGTGTTTCA TCATGTTGCT 540 CAGGTTGGTC TCAAACTCCT AGGCTCAAGC AATCCACCAG CCTCGGCCTC CCAAAGTGCT 600 GGGATTATAG GCGTGAGCCA GCACACCTGC CTTGTCTGGA AGCTTTTAGA GTCACTCACA 660 CAGGAAATGC CGTCTTGGCT CTCCAGGGGT TCATGCTGGA TCCAGCAGAG CAGGACCAGA 720 CAAACACCCG ACATCTTCCC GTTTTCACTC ACCCTCCCTG GCATCATGGT TCAGTGGTCA 780 CGGTGGGCCT GGGAGGGCCC CCCTTGGTTC CCCCTGTTTC CCTTACCTTA ACCTTTGCCT 840 CTCTGACTGA GACCCATTAT GCCTCCTGTC TCTGTTGACT CCATATAATG AAAATAATTG 900 AGCCTGTCTC CACCGATAAC TGTCTCGAAA CAAGCCCCGC CCCGGTCATC TGCCTCTGAC 960 TGAACACACC CCGCCCACTG CACAGGGCCT GCCGTAGCCT GCTTCCAGAA CCCAAGCAGG 1020 GAGAACCCGT AGGCGAGGTG CACGTTTCAC AGTGAATGAA GGAACTGGGG CTGACACCCT 1080 GGTGGACAGC CCTGTGGTTT GCTGAAGGGT GTCTAATGGT TCTGAGACTA AGGTTCAAAA 1140 TCTCTGAAAG CGCCTCTAAA CAAAACGTTA ATTACGGTGT TTTTGCATTT CGACTTTGCC 1200 CTTCATCCTC AGCCTTCCTT CCTCGATGCT TCCTGCCCTG GTTTTGTGTG GAAGATTCCT 1260 TTTTTTTTTT TTTTTTGAGA TGGAGTCTTG CTATGTCACC CAGGCTAGAG GGCAGTGGCA 1320 CGATCTCGGC TCAGTGCAAC CTCTGCCTCC TGGGTTAAAG CAATTTCCCT 1370
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