Tag | Content |
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EnhancerAtlas ID | HS098-10541 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr11:70005350-70007190 |
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 | Myod1 | MA0499.1 | chr11:70007176-70007189 | GGGGACAGCTGGA | - | 6.02 | Stat4 | MA0518.1 | chr11:70006294-70006308 | CGATTTCCTGGAAC | - | 6.13 |
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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 | AAGAGATGGG CCAGGGGTGG CAGCCCCTGT CTGAAGGTGC TTTCGCAGAA GACCCACCAC 60 ACCTCTGCTT GCATCTCATT GGTCAGAACT GTTTCACGTG GCCACCTCCT CTGCAGGGAG 120 GCTCAGGAAT GAGCACACAC TGCCATCTCA GCAAGGCGGG ATGGTAGAGG AAAGACAGAG 180 GATATTGGAT AGGGAAGTAG CCGGCTCTTT TCCCAGCCTT GACGTACTGG TAAACCCCTG 240 TCACAAGGGC TTCATAGGGT TGAAGAGGAC ACAGCTTTGT CTTCAACTTG GGAGTTTCAT 300 TCAGCGAACA AACGTTGGTT GAGCACCTAG GATGTGCCCC ACACGCCCCT GGTCCTGGGG 360 ATGCGGGGGA GATGGACCAG GGAGACTGGA AGGGAGCCTG CTGCAGGGCG TGCCTGTTGT 420 GGGCCCGACT GCCCCATGGC AGGGCAGGGG ACGCGCCCGC TGGGGTGGAG GGCCTCCCTC 480 GCTGAGTCAC CCACAGGCCT GGCGCTCCAG CTGCACCTCC GCATGCTGGC ACGGGGACAG 540 ACATCCTGGA GGCCTCTTGG CAGGACCGAG GGGTTTTCCA AGGAAAGCCC TTGTTCCCCG 600 GAGCTGGCCA GGGAGTGGTC CCCACGCCTC GCAGCAGGGC TTCTCCTTAG TCAGGGTGTG 660 GTGAGGGCTG CAGGCATTTT CCTGGGCAGG GTGCAGTCAC CATGTGTCAC TGGCAGATGC 720 CTGCAGAAGC CGGTGGTAAC GGCCCAGAAC ATGAAATAAG AGCTTTTCTA GGTTTCTGAA 780 AGCTGCAGAC ACCCTCTGGG GCAAACAGAC CCATCCCAGG CTGCAACTGG GAGACACACA 840 GGGCAGCCCC AGGCCTCCTG GGCCTGCCTG TCCTGGGAGC CACCTGTGAC TGTGCCAGCA 900 GGGACCGGAC CTGCCCTCTG CACCCTTGCA TGGGAGCAAA TATGCGATTT CCTGGAACAC 960 GGGGACACAG GGTGACAAGA CAGCCTGTGT CCTGCGGGTG GTTTCACGCC TGGGTGAGGA 1020 GCCTGGCTTT GCTGTGTGCT TCTCCTGCCC AGCCCTCGGT CCATCCATCC TCAATGAGGG 1080 CTCAGAATGG GGCATCCACA CCCCTGGGCA GGGCGGGGCA GGGCAGGGTG AGGGAGCCCA 1140 GACAGACAGA CAGACAGAGG TGTGTGGAAC AATCTTGTCA TTGTAGCCAA CTCCCACCAC 1200 GGTTTCTCAG GCAACCACCA ACCCAAGTTT TATGGAATGT TCTGGTCCCA CGGTATGTTT 1260 GGCAAGAGGA GGGGCTCACT CTGGTGGGAG AGCTAGAAGG GTGCTGCTGG CTGGGAGAAG 1320 GGACCCAAAG CATCTCCAGC CAGACCCAAA GCCCTGCCCC ATCCCAGGCC ACACCTGCCT 1380 CCTTTACCAG GGGAGTCCCT GGGAGGTGGC TGTGAGAGAG GCACACCTCA GCCCTGCACC 1440 ACCTGAGGAT GTCCCTGAGC TCACCATGGG TTGGGGGAGA AGCCCCATCC CGCAGTCAGT 1500 CTGCTCTGGG ACAAGCCACT GGCATGGCGG CCATACTGTG TCCTGGGCTG TGCTTGGGGA 1560 TGGTGCCTGG GCTCCGGGAA GATGGTAGCA CAAAGATCTT GTGAACTGCA GGCTTGGGCA 1620 GACCGCCTGG TAAATCCCAG CTCCTGAGCT GGGTGACCTG GCCTGTCTAC GTAACCTCTC 1680 TGAACCTCAG TGTCCTTGTC CATGGAACAG AAACTAGCCC CTCATCCATC TGTCTCTGGT 1740 GGGTTAATGC ACAGAAAGCC CCTGGCATTT GGCAGGTGCC CAAGAAATGT CAGTGCTTGT 1800 TTTGAAGCAG AAGAGCGGGA AGGTTGGGGG ACAGCTGGAC 1840
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