Tag | Content |
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EnhancerAtlas ID | HS139-45852 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr5:177820930-177822050 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
LHX6 | MA0658.1 | chr5:177821826-177821836 | GCTAATTAGT | - | 6.02 | TCF3 | MA0522.2 | chr5:177821363-177821373 | AACACCTGCT | + | 6.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr5 | 177821773 | 177821834 | chr5 | 177821244 | 177821600 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I178393 | chr5 | 177820848 | 177821961 |
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Enhancer Sequence | TCCCTCTTTT CAACTGATTT TCCAAGGGTG CCAAGGAGTG GGGAGGACCC ACCCCAACCC 60 TGCCCACCAG GTGCCCTGAC AGAAGGATGG GACATAACCC CTTGGTCCCA AGGAAGCAGG 120 TGCTCAGTGT GGCCACAGAC TATCAAACCT GGAGCGAAAG ACCTGGGAGG GCAGGAGGAA 180 GGGAAGCTTC AGGGAGGAAG CAGAGGCAGG ACAGGCAAGG AGGAGGCCCA GGGCTCCAGC 240 ACAGGCAGAG CATACAGTCA CTATCTGCAC CTGTCCTGCC CTGCAGGCCT GGAGCCTCCT 300 GAGGGCAGGT CCGGTACAGG TTTAACCCAT GCCCTGATGC TCAGTCAGCC CAGAGGCTGG 360 CACAGAACAG TGCCTGCCAC ACACTGGGTG AGTCAACCCT GAGCCCTCAA CTCGGAGCCA 420 CTCCCAGCTG GAGAACACCT GCTAGGCTGC ATAGGGCCTG CAGCCCCACC CCAGGAATGC 480 AGAGGCAGCC CCACCAGCCC TCTCTCAGCT CACTCCCTGA AGATCTCCAA GGAAGACAAC 540 TGTATTGACA GCACGGGGTA CTTTTCCTGC TCCAAGAAAT TAACTCATTT CAAAAGCCAC 600 GATGTTCCGG CCTCAACATG GTGTTCACAG CTAAACTGTG TGGCCTGAAG GTTCACATCT 660 TTGGGTAAAC TGAAAATCAT CCTTAGCTAG CATTTGGCTG CAAGTTCAGC CTCCTGGTTC 720 CTGAGTCCAC CCTGACACGC AGAGGGGACT GCTGATGGTC TGACTCCCAT CTGCTACACA 780 TGGGGAAACT GAGGCCCAGA GAGATGGTAT GCCTCCCCAG GGTCACAAGT GGGACATAGC 840 AGGGCTAGAA TTACAAGGCC CTGGGTCTCG GGCAAGGGCT GAGGGGAATT AGTTGAGCTA 900 ATTAGTCATG CTAAGCAGCA TTCGGCTCTC AGCTCCAAAC GTCCAGGCTT GGTTCCGGCC 960 CCGGCTGTCC TCCGAGAGTC TCTCCCCGGC GGGCAGGCGC TCTGGGCATT CGGCTCTCAG 1020 CTCCAAACGT CCAGGCTTGG TTCCGGCCCC GGCCGTCCTC CGAGAGTCTC TCCCCGGCGG 1080 GCAGGCGCTC TGGGCATTCG GCTCTCAGCT CCAAACGTCC 1120
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