| Tag | Content |
|---|
EnhancerAtlas ID | HS091-16252 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr16:10274290-10275730 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| CTCF | MA0139.1 | chr16:10274722-10274741 | CCCCGCCCCCTGCTGGCGC | - | 6.19 | | CTCF | MA0139.1 | chr16:10275582-10275601 | CAGCGCCCCCTGGTGCCCC | - | 6.27 | | SP1 | MA0079.4 | chr16:10274821-10274836 | CTGACCCCGCCCCCT | + | 6.26 | | SP2 | MA0516.2 | chr16:10274717-10274734 | ATCAACCCCGCCCCCTG | + | 6.01 | | SP4 | MA0685.1 | chr16:10274821-10274838 | CTGACCCCGCCCCCTAC | + | 6.26 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AAGGTGAAGA GTGAGAGGCA GGGCCGCGGT GAGCAAGGCG ACCAGAAGAA AGGGATTACC 60
AACTTGGCTT CCTGCTCTAG GAGCCAGGCA TGGAACTCAG CAGCAGGATA GGCTGCTGGG 120
ATCACGGACT CCATTCCGAG TCCCCGACGC CATCCACATC CCTCGATCCA TCTCTAACTC 180
TATCCACAAC TCCAATTCGA GCTAATTCTC CATCCCCCAG CCCCTTCTCG CATCCAGCTT 240
CCTCATCCCC TGTCTCCAGG CACTTCCCCA TCCCCATCTC TGTCCATATC CCCCACCGCA 300
TTCCCCAAGT TCGCCGCGGG CCACAGACCC TAAGCGCCGC GCGTGTTCTG TACCCCACCA 360
AGCTCCTAGG TGCACAGAAT AAACCCTCCA TCCAACCCCT CCCACCTGGG ATAGAGAGGA 420
CCAAGTTATC AACCCCGCCC CCTGCTGGCG CGGAGCGAAC TACAGACCCC GCAGGGCGTG 480
CGGAGGCGGC ACCCAGACCC CGCGTCCCAG CTTGAGAGCT CAGCTAGTTG GCTGACCCCG 540
CCCCCTACGA GCCCGTCGTG TGCACCACAC ACTTTGCTCT ACGCCCAGCC CCAACTACAG 600
ACCCGGCTCC TCTCAGTCAG AGTACACCCC AAGTGCTTGG GAGTGAGGAC GCTGCCTGGT 660
GGGCCCAGGC TCCGCTGTGC CTGGGGAACT TGGGGCTCGC CCCACCTCGA GCCAAGGGGC 720
CGTGGAGAGT CCTTCACCCC TACACGCGCG CGTGCACACA CACGTGCACA CACACACGCA 780
CACACACATG TTCACACACA CACACCCTCT CTCACGCGCG CCGTGTGCAA TGCTGAATTC 840
TGGAGAGTAG GCGCGTCCCC CCGCGGGCCA GCGCGTAGGA GCTGGCAAAG AACGTGCGTA 900
GGGGGAAAGG TAGGCTCCCA AGAAGCTCCC AGACGGACGT GGACTGTACA GCCCCTCCCT 960
AGCCTTTCTA CTGCGGGCGC TGTTGCCAAG TCCTAGGTGC ACGTGGGCAG TGGGCCGCAC 1020
ACGCTCATAG GCACGCGCGC TTTTCTGCGC ACTTCCTCAG ACTGCTGTAG CGGTGCCCAC 1080
GGCCAGCCGG AGTCCTCACA TGTCCTCAGG TGGTGCACAC GCATGAACTG CGGCAGGTGC 1140
ACAGCCCTGC GTACCTGCAA ATACCAGCAC GGTCGTGCAC GCGTGCCCTG ACGCGCGCCT 1200
CTCGGGACGG ACGCTGCTGG AGCCGGGGGA AGTTGAGGCG AACTCCAAGA GGCCTCGACG 1260
TTCCTGGGTA AGCGCCGCGG AGCGCGGAGC CGCAGCGCCC CCTGGTGCCC CTCCTGCACT 1320
TCGCCGCTGG GCTCCCTCCC GCTTTCCCTC TCCCTCTCTA GCCTGATCCC TCTCCCGCTC 1380
TCCCTCCGGT CGAGTCTCCC TCCTCCCCGG CCCAAGGAGC CCTGATCTCC CTCTGGGACG 1440
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