Tag | Content |
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EnhancerAtlas ID | HS051-26039 |
Organism | Homo sapiens |
Tissue/cell | Fetal_thymus |
Coordinate | chr8:22976300-22978550 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
ZIC3 | MA0697.1 | chr8:22977490-22977505 | TCACAGCTGGGGGTC | - | 6.01 |
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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: 4 | ID | Chromosome | Start | End |
GH08I023118 | chr8 | 22976401 | 22976550 | GH08I023119 | chr8 | 22976714 | 22976913 | GH08I023120 | chr8 | 22977721 | 22977870 | GH08I023121 | chr8 | 22978101 | 22978250 |
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Enhancer Sequence | GTTGGTAATA TATTTGTATG GCTTAGGTCA TGTTACGCGC ATCACCCCCT CACCCCATGT 60 CTGCTGTTGG GTCTCAGCAC TGGGTGGAGG GAGGGGCAAT AGTCCTGGTG AAGAGGAGGG 120 GGGAGCGGCA CCAGCTGGAG TGGGGCCTCT GCCGCTGCCT CTTCCTGCTG TGGTTTCTCC 180 GGCTTAGACT GCCCCTCTCA CCTGGCTTGT CTGTGGGGAG ATCTTTGTTC TCTGGCTGCT 240 TTTAAGACTT TCTCCTTAAC AGTGGTTTCA GCAATTCGAT TGAGGCAAAA AGGAGCTGCA 300 GAAGCCATGT CTGTAGCATT TGTGGCCTCC CCTTCTGTAT AATAGCAGCC ATGTTTTGGC 360 CTCTGCAGGG CTAAGGTCCT CTGAGCAGCT GCTTCTCCAC ATCTCTGCCA TGCACTCGGC 420 CTCGGAGCTC CTGGTGTTCC TCAGCAGAGT CCACAGGGCT CTTTGGGGTC CCCTCCCTGT 480 GCTGTAGCCT GGAATCTGTG ACCTGAGGCG GTGAGCTGAG GCCACCACTG GGCTCACCTC 540 ATGGGCTTGG AGGGAAAGTC ACTCCCCCAG GAAGTAGGTG ATGAGCCCTT TACTCTGAGA 600 ATGTCTGCGC CTGGTGGTGG TGGGAGGACA AATGAGCCCT GTGTCAGTCC TGCTCCCTGA 660 AGCCCACAGT CTGGTGGAGG AGGTGTCACC AGGGACCTAA ATAGCTATCA GGAAGCATGG 720 GGGCCACCTC CCCGCTCCCT GCACCTCCAG AGAGACTGCC GGCTCCAGGA ATGTCATCCC 780 TCCCTACTTG ACTCTGGCAG AGGGAGGCTG TGCCGTTGCA AGGCCCCAGG TCAAGATATT 840 GGTGGCCTGG AGGATGTGAT TTCATTAAAA TCAACATTGA GGGGAATGAT TGTACTAACA 900 ACAGCATGTG CTGAAATACA GTACTTGCGC GTGCCAAGCT CTGTTCTCAG CACTTTATAC 960 ACATATGAAC ACACTTAATC CTCATACAAC CAGACTGTAC AGGAACCCTC ATTGTCCTTG 1020 TCTTAGACAA GCAGCGTGAG ACGCAGAACA TTCGTTCAGT GGAGGGGCTG GGCACGGAGA 1080 TGAGTGACCC TCAGGGGCAG CAGCAATGAT TGGGTCACTG GGTTCTGCTG ACCTTTCCCA 1140 GGGGAGTATT TGGTGCTTGT TCGTGAGGCC TGCATTCACC TAGCGCTGGG TCACAGCTGG 1200 GGGTCCCTGA GAAGTCATTT AAGGTCACCT CTTATTTCAG GAATGAAACA TATTTAGATA 1260 AGAAGTGGCT TCCCCTGGAC CGTGATGCTG GCCCAAGACT ACAAGACAGA TGGCTTGCTT 1320 CTTAATCCAA GGTTCTTCTT ATACCAAAAG AACAAAGAAA GAAAAAAGCC ACAAAAGACT 1380 CAAAAGAAGC AGATTTCCCA CCACAGCACA ACCTCAGAAC AATTCTGAGT TGCTCATTTT 1440 AAGATCAACG AGGCATTTTT AGGGCATGTA TGCCTGAGAG AGGAAATCAA TGTGAACGGC 1500 AAACTTCCCT CTAAAACAGC CTAATACAAC ACTGGTCCAG GAGGAACAAG GCAAGGAAAC 1560 CCCCTGGTGA ATGACTCATC TCAGGAAGAG GCAGGGCAGG GTCAGGAGAG TCTATGGAGG 1620 AGAAGACCTG GAACAAGACC TCTCTCTCTT GCTCTCTTAC ACACACACAC ACACACACAC 1680 ACACACACAC ACACTCTCAC ACCCCTATGA GCCCAAATCT ATGAATTGAG AACCTCATTC 1740 TCTGACCTCA CCTTCCATCT CCCTCAATCA GAGATGCCCA CAAACCTCAG AGCTGTGTCC 1800 CAGCATCACT TGTTTTGACT CCCGTCCCCA ACTGCCTTGA CTTCCTGTCT GCCTGGGAAC 1860 CTGTCTGTGT GGACTTTTCC CTCTATGTCC ACCAGTGTCC TGTCACCAGT GGCATTTGTC 1920 ACCTCTGCCT GGGCAGCCCC ACATGACTCT TTGCACCTTC ATGGACTTTG GGGTTATTGA 1980 TGTATGTGCC TCATCTCCCT GTGAACTGGA ACTGTCCTAA GGAAAGGGAG GGTCGTGCCT 2040 TATTCCTGAT ACTCCACGAT TCCTTGTATA GTGTGGCCAC CAGGCACTGA CATGCTCTCC 2100 TTGGATGAAT GAGTACTGTG GGTTCTAGGA AGCCCGCATG AATGCAGATG TGATGTCCTC 2160 AGCCTTTCAT AGACATGTTT CATGTGAGAG GTGGGAAGAG CAGCTGAACA GAAGGCTGAG 2220 GACTGCCCAG GTCCAGAGTC ACCAAGAGCT 2250
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