Tag | Content |
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EnhancerAtlas ID | HS034-05562 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr11:70004850-70007040 |
SNPs | Number: 2 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL2 | MA0478.1 | chr11:70005831-70005842 | CTGAGTCACCC | - | 6.02 | JUNB | MA0490.1 | chr11:70005831-70005842 | CTGAGTCACCC | - | 6.02 | Stat4 | MA0518.1 | chr11:70006294-70006308 | CGATTTCCTGGAAC | - | 6.13 | YY1 | MA0095.2 | chr11:70005283-70005295 | CAACATGGCTGC | + | 6.14 | ZNF263 | MA0528.1 | chr11:70005329-70005350 | GAAGAAGGGGAAGGGTGGGGG | + | 6.2 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I070154 | chr11 | 70001071 | 70007166 |
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Enhancer Sequence | CAGTAAGAGG GACGCTGGCC GACATAAAGA AGTCCAGAGG AGGGTGGCCT CAGTGGTGGG 60 GCCTGCTCAT CCCCCTTACC TGGAGAAGGG GACCCCCTCG GTGGGGGCTG GGGGCTGGGG 120 GCTGTTGTGC TCTCGGTGAC TTGGTGGGAG GGCACCCGGC CTCGTGCTGA GGGGATGTGT 180 CCCCTCTGGC CAGGTGCCAG GCTAGGGGGT TGGGAGATAA CCGGAGCCTC CCCATCCCTC 240 ACCCAGGGGA GGCTAGCCTG AGGTTCAGCC ACTCCCACTG CAGAAGCAGC AGCATTGTCG 300 CAGAAGGGCC AGTGCGGGGC CGGGAAGGAG GTGGCCGTCT AGGGCTGGTC TGGTGGCCCC 360 ACGATGCCAT CAGAGTCACT GGCTTCTCTG ACCTTCTGCT AGCCTGTCCT AGGAGTGGGT 420 CCCCTCTTGG TCACAACATG GCTGCTGCAC CTCCAGCATC ACTTCCACTC TCCAGGCTGG 480 AAGAAGGGGA AGGGTGGGGG AAGAGATGGG CCAGGGGTGG CAGCCCCTGT CTGAAGGTGC 540 TTTCGCAGAA GACCCACCAC ACCTCTGCTT GCATCTCATT GGTCAGAACT GTTTCACGTG 600 GCCACCTCCT CTGCAGGGAG GCTCAGGAAT GAGCACACAC TGCCATCTCA GCAAGGCGGG 660 ATGGTAGAGG AAAGACAGAG GATATTGGAT AGGGAAGTAG CCGGCTCTTT TCCCAGCCTT 720 GACGTACTGG TAAACCCCTG TCACAAGGGC TTCATAGGGT TGAAGAGGAC ACAGCTTTGT 780 CTTCAACTTG GGAGTTTCAT TCAGCGAACA AACGTTGGTT GAGCACCTAG GATGTGCCCC 840 ACACGCCCCT GGTCCTGGGG ATGCGGGGGA GATGGACCAG GGAGACTGGA AGGGAGCCTG 900 CTGCAGGGCG TGCCTGTTGT GGGCCCGACT GCCCCATGGC AGGGCAGGGG ACGCGCCCGC 960 TGGGGTGGAG GGCCTCCCTC GCTGAGTCAC CCACAGGCCT GGCGCTCCAG CTGCACCTCC 1020 GCATGCTGGC ACGGGGACAG ACATCCTGGA GGCCTCTTGG CAGGACCGAG GGGTTTTCCA 1080 AGGAAAGCCC TTGTTCCCCG GAGCTGGCCA GGGAGTGGTC CCCACGCCTC GCAGCAGGGC 1140 TTCTCCTTAG TCAGGGTGTG GTGAGGGCTG CAGGCATTTT CCTGGGCAGG GTGCAGTCAC 1200 CATGTGTCAC TGGCAGATGC CTGCAGAAGC CGGTGGTAAC GGCCCAGAAC ATGAAATAAG 1260 AGCTTTTCTA GGTTTCTGAA AGCTGCAGAC ACCCTCTGGG GCAAACAGAC CCATCCCAGG 1320 CTGCAACTGG GAGACACACA GGGCAGCCCC AGGCCTCCTG GGCCTGCCTG TCCTGGGAGC 1380 CACCTGTGAC TGTGCCAGCA GGGACCGGAC CTGCCCTCTG CACCCTTGCA TGGGAGCAAA 1440 TATGCGATTT CCTGGAACAC GGGGACACAG GGTGACAAGA CAGCCTGTGT CCTGCGGGTG 1500 GTTTCACGCC TGGGTGAGGA GCCTGGCTTT GCTGTGTGCT TCTCCTGCCC AGCCCTCGGT 1560 CCATCCATCC TCAATGAGGG CTCAGAATGG GGCATCCACA CCCCTGGGCA GGGCGGGGCA 1620 GGGCAGGGTG AGGGAGCCCA GACAGACAGA CAGACAGAGG TGTGTGGAAC AATCTTGTCA 1680 TTGTAGCCAA CTCCCACCAC GGTTTCTCAG GCAACCACCA ACCCAAGTTT TATGGAATGT 1740 TCTGGTCCCA CGGTATGTTT GGCAAGAGGA GGGGCTCACT CTGGTGGGAG AGCTAGAAGG 1800 GTGCTGCTGG CTGGGAGAAG GGACCCAAAG CATCTCCAGC CAGACCCAAA GCCCTGCCCC 1860 ATCCCAGGCC ACACCTGCCT CCTTTACCAG GGGAGTCCCT GGGAGGTGGC TGTGAGAGAG 1920 GCACACCTCA GCCCTGCACC ACCTGAGGAT GTCCCTGAGC TCACCATGGG TTGGGGGAGA 1980 AGCCCCATCC CGCAGTCAGT CTGCTCTGGG ACAAGCCACT GGCATGGCGG CCATACTGTG 2040 TCCTGGGCTG TGCTTGGGGA TGGTGCCTGG GCTCCGGGAA GATGGTAGCA CAAAGATCTT 2100 GTGAACTGCA GGCTTGGGCA GACCGCCTGG TAAATCCCAG CTCCTGAGCT GGGTGACCTG 2160 GCCTGTCTAC GTAACCTCTC TGAACCTCAG 2190
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