| Tag | Content |
|---|
EnhancerAtlas ID | HS080-14936 |
Organism | Homo sapiens |
Tissue/cell | H9 |
Coordinate | chr17:47515470-47517940 |
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| Sox3 | MA0514.1 | chr17:47517532-47517542 | CCTTTGTTTT | + | 6.02 | | TFAP2C | MA0524.2 | chr17:47517229-47517241 | TGCCCTGGGGCT | - | 6.11 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH17I049438 | chr17 | 47515458 | 47518162 |
|
Enhancer Sequence | AGCACTTATC AAAGCTTTGA CGCAGTTCTC TGGTGCAGCC ACCTTCTAGA GCTTTTGGTG 60
CACTTCTGAG GCTCCCCTCC ACCTCTTCTG TTTCGAGGAC CTTGGTGGGC TTTGATGGAG 120
ACAGAACCAA GAACCCAGCG CCAAGGTCCA GGCCTTTGTG AGGTGCTGGT GCAGGGGTCG 180
CACACCCAGC TGCCAATCAA GTGAAGGGAG GGAGGAAAAT GAACATCTAA GACCTCAAGC 240
TGGAAGAAGT CTCAGTCCCA GAAGGTGGTA ACTGGTTCCC CTGCCCCTCT TCCTACCCCC 300
TCCCACAGCT CGGCCAGCTG CTGGAGGGAC GCTGCAGGGG AAGGAGGCAG GGTGATTAAG 360
AGCTCTGGTT GTCAGGGCTG GGGCCAGGGG GCACGCCCCC TGGGTGACAT TTTCTCGCAT 420
TGTGTCCTCA GAACAAAAAC GAGTCTTATT TGAGGAGCTG GATGGGGGAG GGGGCCGGGG 480
GGCTGAAGCG ACCGAGTGGA ATCGTGGCTC CAGGGAACAG CGATTACTCA TCAAAGGCCA 540
GGGCAGCCCA CGTCTTTGTG TGCCCTCCGC AGCCCGCCCG TGCCTGGCCA CAGGCCCCCA 600
GCCCTAGACA TCCCCCTGAC GGCCCCCAAA GAGCAGGGCT GGGGTGGGAG AGACCTGGGA 660
TCGTGTGTGG GCACAGAGCC GGGACAGGCG CGGTGGGGGC AGGGGTGACC AGGGCAGGCT 720
TCCTGGAGGA TGGGAGTGTG GAAATGCACA GGACAGAGGG GAGGCGCAAG AAGGAGAACG 780
GCTGCAGGCT AAGGGGGAAA AAAAGTGGGT CTCCGGAGAC CAGGGGGTGA GTGCAGGGGG 840
ACGGGGAGGG GGCAGAACTT CTAAGGTGTC AACTCAGCCC CCGGATGGAG TGTCCTGGAG 900
TGCTTGGGGG AAGGGGCCGC TTCCTGCTAC AATGGCTATT TTGGGGCCTG AATCAAATCA 960
AATCCGCTGC AGCCCCCAGA GCCCCCAGCA GCTGCGCAGA ACAGCTGTCC GGCTGAGGGC 1020
GCTGAGCGGC TGGAATGGCA CTTCCTGCCC CCCACTGATC TCTGGCTGCC CAAGGGTGTG 1080
CGTTGCAGGG GAAGGGGGAA GAGGATGTGA AAGGGCTTTG GGCTCAAGTC AGAAACCTGG 1140
GCTAAGATGG TGTGCTTTCC TCCTCCTGCT CTGTGTGACC GCGGGGCTGA GACTGGCATA 1200
GAGATGCCAG TTCTGGGGCC ATCCTGAAGC TCTTCCCTGC ACCTTCACCC TCCATTCAGT 1260
CCCTACAAGG TATCTCCCCA GGCCCAGACA ATCCCTACCT GAGCAGTCCT CCTGATCTTC 1320
CCCCCAGGAA GCCCTTCTAG TTTCTCTTGA TGGGAAGAGC CCTTTCCTCA TCTGCCGCCT 1380
CCCAACCTCA AAGGCTGTTC CCAGACTGGT TCCCTGCAGG CAGAGGAGCA TCTCTCCCAT 1440
CAGATCTGGA TTTGGTTCTT CCTCTAGCTG AACTCCCAGC CATCCACTTG GTATTTACTC 1500
ACAAGGCACC TGAGGGTTGA CACGGAAGAC AGGTAAGCTT CCCGGCAGGT GCCTGTTCAA 1560
TCTCCTGATT GTGCTGAAGG GGCCTCATGC ATGCCAGCTA AAAACCCATA GGCTGGCATG 1620
TAATAGAGTT GGGGGGAGCA CTGAACTGCC TCCTCCAGGA AGCCTTCCTG GGACAGGCAA 1680
AAAGGAGAGG TCTCTTTCTT TTTGGTCCAC CCTGGCTCAA GGCCAGCCAA TGTCCACAAG 1740
AGTGACCAAA GCTAGGACAT GCCCTGGGGC TGCCATGTCC CTCAGGTCAC TAGTCCATGA 1800
CGGGGTCCCT CGTGCCCATC TTGTGCAGAA AGAACCCCAT TGTCCAGGGG GCATAGCTGA 1860
GGGGTGAGTT CAGAGCCCAG AGATGTTGAC CACAGGGCTG GTCATCAGTC TTCTGACCAC 1920
AGCAGGAGGG AGTTGGGGAA CTGTGTGGTC TGTGGGGGTG AGGGGCAGGC ACACACTAGT 1980
GCACACACAG GACCATAAGC CCAGACACTG CCCTCCTCAT CCAAGCACAC ACTCCCCCGT 2040
GCTCCCCCCA GGACGGCCCC TCCCTTTGTT TTTCCGCATT CCTGCTGGCA GATGCTCCAT 2100
TCTTTTCTTC CCCAAGCAAG CCAGGGAGAT CTCCACCTTC CGGGGTGGGG GGGCTCCGGA 2160
CATAGCAAAA GTGGGGGGAA GCAGGGATGT GCCACCTGTC CCTGGGGGCA GGGGCAGCCC 2220
CTGGAGCCCC ACCCACACTG GGATGAGAGC CCAGGGTGCT TTGATCTCCT GTGCGGTGCG 2280
CCTGTTGTGG AAGCTGCCAA GATTAACAGA GATGCACACA CAGGTCTTTT AGCCAGGTCT 2340
GCAATTCCTG AGCTTGTTTC CAGATCAGAG CCCTCATCTT CCTTCAGAGA CCTCTTCACT 2400
AATGGACCTC CCACCTCTTT CCTCACTGAA TCTCTCCCCT CATTGAACCC CCTCTCCTCT 2460
CCCATCCCTA 2470
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