Tag | Content |
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EnhancerAtlas ID | HS059-26995 |
Organism | Homo sapiens |
Tissue/cell | GM12878 |
Coordinate | chr2:178145880-178147990 |
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) |
Foxd3 | MA0041.1 | chr2:178147938-178147950 | GAATGTTTGTTT | + | 7.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26714 | chr2:178146124-178148074 | Esophagus |
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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 |
GH02I177281 | chr2 | 178145928 | 178147728 |
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Enhancer Sequence | CTGCCCGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGCCCGGCAT 60 CCTTCCCTTC TTTAGTTTAC ACACATAGGC CCCAGGTACA GGGCATGAGC TAGAGCTGGA 120 TCCCAGCTGA ATGGAAAGCA GGAGGCGCTA TATTGGAAAC AACTGCCAAG CAACCAAGGA 180 CTGGGGACAA AATAGCCTGG GAGGAGAAGT AAAACCAGGA AAAAGTTTAA AATTAGGTGC 240 CTGACATTTA AGGGAAAAAG TCCAAAGTTA ATCAAGGATG ACCGCTTATT GCAAGATTCA 300 AAACCTCTAA ATGACAAAAC TTCTAAAAAA GGAAATGATG ATAGCACGGG GAACCCTGCT 360 GATCCATCTC CCTGCCCAAA TACTTCTCCA TTCCCAACAT CTGTGCAGCC ATGTGCAGCA 420 GAGACAAACA GCAGCAGCAC TCCACCCCCA AGCTTTGAGA ACCGCAGAGC TGTGGCTGAC 480 ACAGTGGTCC TATCTCTGTG AAGTACACAA ACCATACCAC AGCCTTATTT TCTGAGACCA 540 TCTCTATGTA ACCAGCTTCC CTAAATGCTG TGGCCCAAGA GGCTAACACT TTGGTCAGTC 600 ATGGGGCAAT ATGGCTGCTC CCACATGGCA TCCAAGTCCA TGCTTAGAGA CTGAAGGGGA 660 GCCAGCCTTG GTAAACCAGG TCTGTGGTCA TTTCCCCACC TGGCATTTTT GAGCTGTACC 720 AAGCAGCCTA GGGGTTCTTA CTGCAAGGGC ACGCTCAAAC CTGACTTGTC CAGACAAGCA 780 GAAGAGTTTT GGGCTCCCAA TCGAGCACGG TGGTCAGTCT GTTCCAGTTT GTCTGGGACT 840 TTCCAGGTTT GAACACTGAA AGTTCTACAG CCAGGAAATC CCTCAGTCCC AGGCAAACTG 900 GGATGGTTGG TCACCCTGAA GTCAAGACAC CTAGGCTTTG GCACCTAAAC ATCAGTTTCC 960 TCATCTGTAA AATGCTGGGA CTGGCCAGTA CAGCTTCTGA TGTTACTGCC ACATCTAATA 1020 GTCCATGATT CACTCTCATG CTCCTGACCT TACCCATCTG CAGCCCAACT CCCAAACAAA 1080 CTTCACTTGA TCCAAGATCG AGTTCATGTA ACCTGATAAG CTAATCATTA GTGTGTTAAC 1140 AGGAGAGGAT TATAGGGTTC ACAGTTGAAT TTTAACAATG GCTCGGGTGG AAGGCATGTG 1200 GGTAGCTGAG TCGTTCTAAT GGTGGGAAGT TCAGCTGGGG AGATGGAGTG TATGGCTCTG 1260 TGCCATCTGA GAGAAAGATA TTTTTAGGCA GGCAGGTTTT GAGGCAGCCA GCCTGAGAGA 1320 GCTGGTTTGA TGGGCTGCTT TTAGCTGCAC AGCAGGAACA GGCCACAGGC AGGGCAGTCT 1380 TGTCTGACTT GAGCCAACTT TCACACTATG ACCTGAATAA AATCAGCAGT TGAAGCCACA 1440 GACTGGAGAA GAAAGGATGT AGTCTGCTGA TAGCAATATA TATGTATATA ATGCATTTGC 1500 TTTGAGCCTG GGTCTGTCAT CTATAATACA GATATGTAGC TATGATCCTG GGTAGTTGAG 1560 AGTTCAGACT CTGGGATCAC CACCTACCAA CTCTGTGATA TTGGGCAAGT TGTAGACTGA 1620 ATAATATGCA TTTGCTGATA TTTAACCTTT TTGATCTACA CACACAGGAA TTCCACGTGG 1680 TTTAGCCTAA TAGCTTACTC TCTTTTTCCT TGGTTTCCTC ATGTGTGAAA CGCAGATAGC 1740 CACCAAACTT TTCAGGACAC TGTGAGGACC AAATGAGAGG GACACATAAG GTGGTCAGAA 1800 CAGTCCTAGC CCCACAGTCC ATGTCAGTGA TGTCAGCCAC CACCATCCTA CTGGTGAAGA 1860 GGCAGGCATA CAGGGCCATT AGACTCCATC AGCTGAACCT AGGGTAGCCC AGACTCTTCC 1920 TGTCTTCCTG AGACATGGAA CATGGATGAA CCAAAGTGAA TTGGTCACCT TAGCTGAACT 1980 GTAGAACTTC ATTCTAATCC CAGGGTGAGG AAAGGGGAGT AGGTTCATAC CACAGGTTTT 2040 TCAGGTCATT CCAAGACTGA ATGTTTGTTT TTCCTCCCAA TACAATCAGG TCCTAAGTAT 2100 AAAAAAGAGC 2110
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