Tag | Content |
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EnhancerAtlas ID | HS076-10487 |
Organism | Homo sapiens |
Tissue/cell | H1 |
Coordinate | chr11:64115590-64116800 |
Target genes | Number: 43 | Name | Ensembl ID |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr11:64116152-64116165 | GGCAGCTGTCCCC | + | 6.29 |
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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 |
GH11I064347 | chr11 | 64114902 | 64116804 |
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Enhancer Sequence | GCTTGGGGCA ATGCCTGGCA CCTAGAATGG ACCTGTTCCA TGGGAGGGAA TGGCAGCAGG 60 TAGGCAGTGA AGGTGAGGGT AGGGCTGGCG GGCTGGAAGA GCCGGCTCCA AGGACTGAGA 120 GGGTGGGGGA AGCTAGGGAC AAAGGGGGAA TTTTGTGAGA TTTCCTGGTT GGAGCAGGAG 180 AAGGTGGCTG GCCAGGGGGA GGTCAGGGAA CCAGGGGGTC TCAGGTTGTC CACTGGGTGG 240 GGAAGCCTCC CAGGCTTGGG GGAGGGGGTT CTAGGAGGGC TGTGGCCAGG GCCCGGAGGA 300 GGGCAGGGCA GGGGCTGGGC GGGAGGTTCT ATTCACCGTG CCTCCTACCC CAGTACTTGC 360 GCTAGTGGCT GTCAGCCAGC CAGGCAGCAG TGCCTCATCG GACTTGTAGT TTTTCAGGGA 420 GAGGTGGTGG CCAAGAGTGT CAGGAGGTGC AGTGCCCCTT GGGCAAGGCC TAGGTGCAGT 480 TATTAAGCCA GGAAGGTAGT TTTCAGCAGC AAGGCTTGTA GGCTTGGTTT CCAAGGCAGG 540 ATTTGGCTGG CAGCTGGTCA TGGGCAGCTG TCCCCGAAGC TTCATCCTGC CAGGCCCCCC 600 ATGTGGCAGA ATGGTTTGGT CTCCCTCCCT CTGGGGCACA CAGGCCAGAA TGGGCCTCCC 660 GTCTCCTTCC AAAGTGGTGC AGCCCAACCG CCAAAGGCCA CAGGTCACCT AGCTGGCAGC 720 ATCCTGGCGC CCCCTGCCCC CCCAGCCCCC ACTGTCAGCT CCTGACTTCC TGTCCCTCCA 780 GCCCTCCGTG GCCTTTTCCC TGTAGCCAAG GTCTCTCACC CGACCCACCT CTGCTGAGCC 840 TCTCTAGCTG TCTCGCTGTC ACATGGCTGG GGTGGCAGCC CACCGGGCGC ATCCACCTTT 900 CACTGCGCAC ATGAAGAACC GTGGGCTCAG AGAGGTGACG GCACTTGCCC AACATGTGTC 960 ACCTACCGAC TCCCAGCCCA GGGGCCTTCC TCATGCCCTG CCAGGCTTAC AACACCCAGC 1020 TCTTTCATGC CCAATTTCAA GGGCCCCAGG CTTTGCTCCC ATTTTATAGA TGGGGAAGTA 1080 GAGCCCAAAG GCTTAATGAT ACGTGCCCAG GATGGCAGGT CAAGGACAGA AAGGCAGCTC 1140 TCTTGACTCT CAGGCCTCTG TCTCCGGCTG TCTCCTGCCC CCTTGCCCTG AGCCTGCTCT 1200 GCTTGCCCTC 1210
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