| Tag | Content |
|---|
EnhancerAtlas ID | HS104-10904 |
Organism | Homo sapiens |
Tissue/cell | HUVEC |
Coordinate | chr11:65782260-65784160 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| NR2C2 | MA0504.1 | chr11:65783774-65783789 | TGACCTCCGACCTCT | - | 7.02 |
|
| | 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 |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH11I066014 | chr11 | 65782167 | 65784451 |
|
Enhancer Sequence | TCTCAAAAAA ATTAAAAATA AAAAAAGAAG AAGAAAACAG CATTGCAACA TTTGCACATC 60
TGAATTTGTG GCTGCAATTC ATACCCCCCC ATACATATAC ACACGCACAC ACCCAAAGCA 120
CAACACACCA GACATACACA CACAGACACC CAGAGCACAC ACTCAGATGC TGGCAGATAT 180
CACATGCATA CCCAGAGAAA CACAGCCTAG CAACTCATGA GCACAGAAGC AACACACCCT 240
AGAGAAACAA CCTGGAGATG TACACACAAA ACTCAAACAC AACCCAAGGA CCCACATGCC 300
ACACCCAGAG GTTCCTCAGA TGCACAAGCA CACACCCACA CTTGGGATAT GGGCCTTGGG 360
GGTGCTAGGT ATAGGCACCA TCAGGCCCAG GCAGGCAGCA CTGCAGTGGC TGCGGAGAGC 420
ATCCCACGGT CCTTCCTTTC TGACAAGGCC TCACACCCTG CTTGTGCCTG CCTGGTCCCC 480
TGCCCAAGGC TGGGGCCTAA TAAGCAGCAG CCCCAGCTCC CAGGCCCTGC TGTCGGCCTT 540
TGGAGGCCAG ATTGGGGTAG AGACGGGGAA ACGGGAAGTA GACCCTGGGT CCCACCTGGG 600
AGTGAGAAGC TGAGGGGTGG CATTTGACAG GAGCTGGGGA CCCAGGAGAC AACATCCAGC 660
CCTGCTTCTG CTCAAGCTTG TCAGATGTGG CAGCTCAGAC AGCCCAGGGT GTGTGCGGGG 720
CCTGCTGCTT GGAAGGGCTC CCATGTGCCA CCAAGCAGGG ACTCCCAGCA TGGGGCAGGC 780
ACAGGGTGGG TGGCAGGAAA TGCCTGTTGA ATGAATGTGT GAGGTGGTGG AGAGAAGCAA 840
GGCCCAGAGA CGCCTGCCCG GTGACCTCTC CGCCCCTGGA ATCTGTGCCC AAATCCCAGA 900
TGGCATTTCC TCCGCATAGT CTATTCCTGG GCCCTGGGCC CTGGGCCAGC CAGTGCCTTC 960
CGCCAGACCA GGGAGGGGAG GTGCTTCTTC TGTCCTGGGA CCCTGGAAGC TCCAGCACTG 1020
ACTGGTCTGG TCCAGAGATG GGAGGGTTGG CAAAAAACTA TTGCCCTTCA GCTCCCGCTC 1080
CTGACTCCCT CCGGCCTGAA CTGCACCCTG GATTCGCCTC TACTAGAGGT GAGATGGCTG 1140
TTGTAGATAA TGGAAAACCC TCCACTTAAG GAGAGACCCC TGGGGCCAGG GCGAGGCTTG 1200
AACTTGACTC AGTGCTAGGT CTCCAGCACC CAGCATAGGC CAGTGTCCCA CTGTCACCCC 1260
CAGCCATGGG GACAGGGGCT CTGGACATCC AGCCTAGGCT CAGGCTATCA GTCGGGGAGG 1320
TCATCTAAGT CCTAGAGCAG GCAATGGGGC GCAGCCTTCA GCCTCATTCC CTGCTTCCCT 1380
CTCCCAGCAG CAGGGTCCTC CACACATCCC TGCCCGCCCC TTGCCCTGAG GCCAGAAGGA 1440
CTTGAGCAGC CCCGACTCCA CCTCCCCTCA GTGGGGCTCT AGAGTCTGAC CCCAGAAAGG 1500
GCAGGATATG GCAATGACCT CCGACCTCTG GGTTCATGAT ATCCCCATCC GGTTGGTGCT 1560
CTTCTACTGG AGCTGAGGGT CCTGGTAGGA TTGAGTTCCT GGGCTCTGAG TCCCCATTCC 1620
TAGAGCCTAT TGGGCCCCCA GGCCCTGGTA ACCCTGGGGT GTTCAGGCCT ATTCTTTTTC 1680
TCCTGACTCT TGGGCCAGAT GGGCCTTCCT CCCCAAAGCA GGGTTACTGC CTCCTCGGCC 1740
CTCCCGGCAC CGCCGGCACC TGAGCTCAGC CCACGTTCTG CTTCATCCCT CCAGCTGCTG 1800
CTAATGCCCT GCTGGGCTGA GCTAGCATGC GGGCGCTGGT AGGGCTGGAG GGGATCCAAG 1860
AGCAGCTCCT TTCACATGCA ACACGGGCAC ACACTCGTTC 1900
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