| Tag | Content |
|---|
EnhancerAtlas ID | HS091-32688 | Organism | Homo sapiens | Tissue/cell | HepG2 | Coordinate | chr22:24637980-24640520 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| STAT3 | MA0144.2 | chr22:24639552-24639563 | CTTCTGGGAAG | + | 6.14 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 2 | Chromosome | Start | End |
| chr22 | 24638000 | 24638837 | | chr22 | 24639816 | 24639909 |
| Enhancer Sequence | CACCATGTTG CCCAGGCTGG TCTCCAACTC CTGACCTTAA ATGATCCACC CGCCTCAGCC 60
TCCCAAAGTG CTGGGATCAC AGGTGTGAGC CACCACACCC AGCCAAAAAT CACCTTTTTT 120
ACAAGGATCA AAACAGTCAT TATGCTGGAG ATAACAGACC TCACTGTCAC CATGCTCCTT 180
TTGTATGTCT ACTAGGCACG GTGCTGGGTC CACACTCACA GAAAGCTTAG GAGCTTGCAC 240
CCAGGGGCTC CGGCTGTAGC AGAATCCCAA GAATAAAACC TAGTGCTGAA AGAGTAGGAG 300
ATGGGGCTGG GTGCCGTGAC TCACTCCTGT AATCCCAGCA CTTTGGGAGG CGGAGGTGGG 360
CAAAGCACGA GGTCTAGAGT TGGAGACCAT CCTGGCTAAC ATGGTGAAAC CCCATCTCTA 420
CTAAAAATAC AAAAATTAGC TGGGCGTGGT GGCTAGCACC TGTAGTCCCA GCTACTCAGG 480
AGGCTGAGGC AGGAGAATCA TTTGAACCAA GGAGGCAGAG GTTGCAGCGA GCCGAGATCA 540
TGCCACTGCA CTCCAGCCTG GTGACAGAGC GAAACAGCAT CTCAAAAACA AAACAGAAAA 600
AAGAGCAGGA GACTGGACTC TGGGAGGGCC TCCTGGTGAG AGGTGAGCAC AGAGGGGAGA 660
GATGATGGAG TCAGGAGCAT GGGCTTCTGG TGGCCCCAGC AGACCCTGTG GCAGTGTGGC 720
CAGGGGCCTC TGCAAGGAGG GATCTTGGCC AGGATGACGC TGCAGCAGGC CTCTTCCTGA 780
GGCCCCCCAG CCAGTCCGGC CAGGGTCCCA GTGTCCAATG ACCCCTGTTC CGCAGCAGCA 840
GCTGGGGCCA GCCCCAGGCT CTCTTCCACT CCCAGCTTCT TAAGACAGGA AGTGGAGAGA 900
GTTGTTTGAC AAAACACTGG GGCAAACCAC ATCCTCTCTC TTCAAGGGAC AGTTTGAGGG 960
GATGCCAGCA GAGGGAGCTT TAGAGTAGAG ACCCCTACCC AACCAGTGAC CGTCACGCAC 1020
ACAGCAGGGC ACGCTATGGA GACCCCCAGA CAGTCACTCA GGGAGACCCA GCAGGTCCAG 1080
ACTCCACCTA GAAATTTGTG GCAGCAGGTC CCCACTCCCA AAGGCCACAT GCCCACGGGT 1140
GGTCTCTGGT GCCTGAGACT CCAGTCTCAT TTGCATCTTT GCAACTTCGA GTTTAAGTGG 1200
GTGTCGCATC CTGAATGTCC TCCTGAGCAG AGGAGGGGCA CAGCCTGGGG TGGCGGCTGG 1260
CGTCAATCCC TCAAATCCCC TGAGAGCCAC TGGGGAGACT AAGCAGTCCC CAGCCCCGAC 1320
TTGTCCCTGA GCTGCCATTC TCAGCCCTGT GGGAGGAGAC AGAAAGACCT GAAGAGAAAC 1380
CAAAGGACCA GGTCAGGAGG GGCGGGGGGT GGCATGAGAA ATCAGGGCAG GGAAGGATGG 1440
ACAGATGGGG GAATGGAGGG AAGAAGGAAT GAATGAAAAG GTGAATGAAT GAACAGAGAG 1500
AGAGAGCAGC CACTCCTCCC TTGCTTTAAT TTACAAAGCA CTGGGATCCT CCCAACAGCC 1560
TGCAAGACAG AACTTCTGGG AAGCAGACCA GGTGGCTGGC AGGGAGGGGA GGCTTGCCCT 1620
GGCTTTTGTG GGCCCAGTGG GAGGCAGGGA GCAGGAAGGG GCATCCTGTA TGTGTCCTCT 1680
GCAGCAGCAG CAGCGGAGGC CTCCCTTGGG CTGGGCTTCC TGGAAGAGGG TCAGGAAACA 1740
CCCGCTGTGG CCCCTCTCCA CCACGCCCTC ATCCAGGACA CCAAGTATCA GTCACTCAGC 1800
TCACGAGACC CAGGCCCTGA CTCAGGGAGA GAGGATGTGA GGGGTGGGGC ACCGGGCTCC 1860
TCAGGACTGA GAGACCCGAG ATGTGGCCCC AGGCTGGGTG TTGGGGCAGA CTGGCTATGG 1920
CAGCATTGTG TGTACCCCAG CAGGCCAGTA CCCACGCAGG GAGCCTCCAA ACCCCTTCAC 1980
CCATGACCCT GGGAGAAGAC CGCAGCCTTG GAGAATTGGC CTCACTGAAG GGGCCTGCAC 2040
CGGCCAGCAG GGTCAGGCGG GGCCAGACAG GTTCCCACCT GGGATATGCA AATGGGCCTC 2100
CTGAATCCTG GAGCCAGGCG TGGACTCACA CACCACCATT GTCCCCAAGT CCCCATCTGC 2160
CCCACGAGCA CACCCTGCCA CCTGTTCTGT GCAAGGGCCC TGAGGCTGCC TCCTTGCGCC 2220
CAAGACCTGC AGGTGCTGAA GCCCACACAC ACACGGCTCC TGCTTCCTGG GCCAGTGCAC 2280
GTGCACACAC ACACACACAC ACACCCACCC ACACATACAC ATACCCACAC ACAATCACAC 2340
ACATTCACAC ACACCCACAC TCCCCACACT CACACTCACA TACACTCACA CACACCCACA 2400
CATGCATGCA ATCACACATA CCCAGACACT CACACACACA CCCACACATA CATTCACTCA 2460
CACACACACA CACACACACG CCTTCTCCAG GAGGGGCTGG CTGCCAAGGG CCACCCAGCT 2520
TCCTCCCACG TCTCACTCAC 2540
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