Tag | Content |
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EnhancerAtlas ID | HS098-10338 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:65782290-65784220 |
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: 4 | Chromosome | Start | End |
chr11 | 65783490 | 65783816 | chr11 | 65783906 | 65783950 | chr11 | 65782751 | 65783478 | chr11 | 65782974 | 65783337 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I066014 | chr11 | 65782167 | 65784451 |
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Enhancer Sequence | AAGAAAACAG CATTGCAACA TTTGCACATC TGAATTTGTG GCTGCAATTC ATACCCCCCC 60 ATACATATAC ACACGCACAC ACCCAAAGCA CAACACACCA GACATACACA CACAGACACC 120 CAGAGCACAC ACTCAGATGC TGGCAGATAT CACATGCATA CCCAGAGAAA CACAGCCTAG 180 CAACTCATGA GCACAGAAGC AACACACCCT AGAGAAACAA CCTGGAGATG TACACACAAA 240 ACTCAAACAC AACCCAAGGA CCCACATGCC ACACCCAGAG GTTCCTCAGA TGCACAAGCA 300 CACACCCACA CTTGGGATAT GGGCCTTGGG GGTGCTAGGT ATAGGCACCA TCAGGCCCAG 360 GCAGGCAGCA CTGCAGTGGC TGCGGAGAGC ATCCCACGGT CCTTCCTTTC TGACAAGGCC 420 TCACACCCTG CTTGTGCCTG CCTGGTCCCC TGCCCAAGGC TGGGGCCTAA TAAGCAGCAG 480 CCCCAGCTCC CAGGCCCTGC TGTCGGCCTT TGGAGGCCAG ATTGGGGTAG AGACGGGGAA 540 ACGGGAAGTA GACCCTGGGT CCCACCTGGG AGTGAGAAGC TGAGGGGTGG CATTTGACAG 600 GAGCTGGGGA CCCAGGAGAC AACATCCAGC CCTGCTTCTG CTCAAGCTTG TCAGATGTGG 660 CAGCTCAGAC AGCCCAGGGT GTGTGCGGGG CCTGCTGCTT GGAAGGGCTC CCATGTGCCA 720 CCAAGCAGGG ACTCCCAGCA TGGGGCAGGC ACAGGGTGGG TGGCAGGAAA TGCCTGTTGA 780 ATGAATGTGT GAGGTGGTGG AGAGAAGCAA GGCCCAGAGA CGCCTGCCCG GTGACCTCTC 840 CGCCCCTGGA ATCTGTGCCC AAATCCCAGA TGGCATTTCC TCCGCATAGT CTATTCCTGG 900 GCCCTGGGCC CTGGGCCAGC CAGTGCCTTC CGCCAGACCA GGGAGGGGAG GTGCTTCTTC 960 TGTCCTGGGA CCCTGGAAGC TCCAGCACTG ACTGGTCTGG TCCAGAGATG GGAGGGTTGG 1020 CAAAAAACTA TTGCCCTTCA GCTCCCGCTC CTGACTCCCT CCGGCCTGAA CTGCACCCTG 1080 GATTCGCCTC TACTAGAGGT GAGATGGCTG TTGTAGATAA TGGAAAACCC TCCACTTAAG 1140 GAGAGACCCC TGGGGCCAGG GCGAGGCTTG AACTTGACTC AGTGCTAGGT CTCCAGCACC 1200 CAGCATAGGC CAGTGTCCCA CTGTCACCCC CAGCCATGGG GACAGGGGCT CTGGACATCC 1260 AGCCTAGGCT CAGGCTATCA GTCGGGGAGG TCATCTAAGT CCTAGAGCAG GCAATGGGGC 1320 GCAGCCTTCA GCCTCATTCC CTGCTTCCCT CTCCCAGCAG CAGGGTCCTC CACACATCCC 1380 TGCCCGCCCC TTGCCCTGAG GCCAGAAGGA CTTGAGCAGC CCCGACTCCA CCTCCCCTCA 1440 GTGGGGCTCT AGAGTCTGAC CCCAGAAAGG GCAGGATATG GCAATGACCT CCGACCTCTG 1500 GGTTCATGAT ATCCCCATCC GGTTGGTGCT CTTCTACTGG AGCTGAGGGT CCTGGTAGGA 1560 TTGAGTTCCT GGGCTCTGAG TCCCCATTCC TAGAGCCTAT TGGGCCCCCA GGCCCTGGTA 1620 ACCCTGGGGT GTTCAGGCCT ATTCTTTTTC TCCTGACTCT TGGGCCAGAT GGGCCTTCCT 1680 CCCCAAAGCA GGGTTACTGC CTCCTCGGCC CTCCCGGCAC CGCCGGCACC TGAGCTCAGC 1740 CCACGTTCTG CTTCATCCCT CCAGCTGCTG CTAATGCCCT GCTGGGCTGA GCTAGCATGC 1800 GGGCGCTGGT AGGGCTGGAG GGGATCCAAG AGCAGCTCCT TTCACATGCA ACACGGGCAC 1860 ACACTCGTTC GTGTGTGTGC ACCAATTCCC TTCCCTGCGC CTTGGCCTAG TCAGTGAGGA 1920 CATGGAGCCT 1930
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