Tag | Content |
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EnhancerAtlas ID | HS041-03989 |
Organism | Homo sapiens |
Tissue/cell | EWS502 |
Coordinate | chr11:65781850-65784220 |
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) |
NR2C2 | MA0504.1 | chr11:65783774-65783789 | TGACCTCCGACCTCT | - | 7.02 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 5 | Chromosome | Start | End |
chr11 | 65783490 | 65783816 | chr11 | 65783906 | 65783950 | chr11 | 65782751 | 65783478 | chr11 | 65782974 | 65783337 | chr11 | 65782178 | 65784200 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I066014 | chr11 | 65782167 | 65784451 |
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Enhancer Sequence | GGTAACACGG TGAAACCCCG TCTCTACTAA AAATACAAAA AATTAGCTGG GTGTAGTGGC 60 GGGCGCCTGT AGTCCCAGCT ACTCGGGAGG CTGAGGCAGG AGAATGGCGT GAACCCGGGA 120 GGTGGAGCTT GCAGTGAGCC GAGATGGCGC CACTGCACTC CAGCCTGGGC GCCAGAGCCA 180 GACTCCATCT CAAAAAAAAA AAAAAAAAAA AAAAAACCAG CCTGGCCAAC ATGGTGAAAT 240 CCCATCTCAA CCAAGAATAC AAAAATTATC TGGGTGTGGT GGCAGGTGCC TGTAATCTCA 300 GCTACTCAGG AAGCTGAGGT AGGAGAATCG CTTGAATCCA GGAGGCAGAG GTTGCAGTGA 360 GCCGAGATTG CGCCACTGCA CTCCAGTCTG GGAGACAGAG CGAGACTCCA TCTCAAAAAA 420 ATTAAAAATA AAAAAAGAAG AAGAAAACAG CATTGCAACA TTTGCACATC TGAATTTGTG 480 GCTGCAATTC ATACCCCCCC ATACATATAC ACACGCACAC ACCCAAAGCA CAACACACCA 540 GACATACACA CACAGACACC CAGAGCACAC ACTCAGATGC TGGCAGATAT CACATGCATA 600 CCCAGAGAAA CACAGCCTAG CAACTCATGA GCACAGAAGC AACACACCCT AGAGAAACAA 660 CCTGGAGATG TACACACAAA ACTCAAACAC AACCCAAGGA CCCACATGCC ACACCCAGAG 720 GTTCCTCAGA TGCACAAGCA CACACCCACA CTTGGGATAT GGGCCTTGGG GGTGCTAGGT 780 ATAGGCACCA TCAGGCCCAG GCAGGCAGCA CTGCAGTGGC TGCGGAGAGC ATCCCACGGT 840 CCTTCCTTTC TGACAAGGCC TCACACCCTG CTTGTGCCTG CCTGGTCCCC TGCCCAAGGC 900 TGGGGCCTAA TAAGCAGCAG CCCCAGCTCC CAGGCCCTGC TGTCGGCCTT TGGAGGCCAG 960 ATTGGGGTAG AGACGGGGAA ACGGGAAGTA GACCCTGGGT CCCACCTGGG AGTGAGAAGC 1020 TGAGGGGTGG CATTTGACAG GAGCTGGGGA CCCAGGAGAC AACATCCAGC CCTGCTTCTG 1080 CTCAAGCTTG TCAGATGTGG CAGCTCAGAC AGCCCAGGGT GTGTGCGGGG CCTGCTGCTT 1140 GGAAGGGCTC CCATGTGCCA CCAAGCAGGG ACTCCCAGCA TGGGGCAGGC ACAGGGTGGG 1200 TGGCAGGAAA TGCCTGTTGA ATGAATGTGT GAGGTGGTGG AGAGAAGCAA GGCCCAGAGA 1260 CGCCTGCCCG GTGACCTCTC CGCCCCTGGA ATCTGTGCCC AAATCCCAGA TGGCATTTCC 1320 TCCGCATAGT CTATTCCTGG GCCCTGGGCC CTGGGCCAGC CAGTGCCTTC CGCCAGACCA 1380 GGGAGGGGAG GTGCTTCTTC TGTCCTGGGA CCCTGGAAGC TCCAGCACTG ACTGGTCTGG 1440 TCCAGAGATG GGAGGGTTGG CAAAAAACTA TTGCCCTTCA GCTCCCGCTC CTGACTCCCT 1500 CCGGCCTGAA CTGCACCCTG GATTCGCCTC TACTAGAGGT GAGATGGCTG TTGTAGATAA 1560 TGGAAAACCC TCCACTTAAG GAGAGACCCC TGGGGCCAGG GCGAGGCTTG AACTTGACTC 1620 AGTGCTAGGT CTCCAGCACC CAGCATAGGC CAGTGTCCCA CTGTCACCCC CAGCCATGGG 1680 GACAGGGGCT CTGGACATCC AGCCTAGGCT CAGGCTATCA GTCGGGGAGG TCATCTAAGT 1740 CCTAGAGCAG GCAATGGGGC GCAGCCTTCA GCCTCATTCC CTGCTTCCCT CTCCCAGCAG 1800 CAGGGTCCTC CACACATCCC TGCCCGCCCC TTGCCCTGAG GCCAGAAGGA CTTGAGCAGC 1860 CCCGACTCCA CCTCCCCTCA GTGGGGCTCT AGAGTCTGAC CCCAGAAAGG GCAGGATATG 1920 GCAATGACCT CCGACCTCTG GGTTCATGAT ATCCCCATCC GGTTGGTGCT CTTCTACTGG 1980 AGCTGAGGGT CCTGGTAGGA TTGAGTTCCT GGGCTCTGAG TCCCCATTCC TAGAGCCTAT 2040 TGGGCCCCCA GGCCCTGGTA ACCCTGGGGT GTTCAGGCCT ATTCTTTTTC TCCTGACTCT 2100 TGGGCCAGAT GGGCCTTCCT CCCCAAAGCA GGGTTACTGC CTCCTCGGCC CTCCCGGCAC 2160 CGCCGGCACC TGAGCTCAGC CCACGTTCTG CTTCATCCCT CCAGCTGCTG CTAATGCCCT 2220 GCTGGGCTGA GCTAGCATGC GGGCGCTGGT AGGGCTGGAG GGGATCCAAG AGCAGCTCCT 2280 TTCACATGCA ACACGGGCAC ACACTCGTTC GTGTGTGTGC ACCAATTCCC TTCCCTGCGC 2340 CTTGGCCTAG TCAGTGAGGA CATGGAGCCT 2370
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