Tag | Content |
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EnhancerAtlas ID | HS098-39887 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr3:126690100-126691280 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr3:126690898-126690911 | TGCAGCTGCTCCC | + | 6 | STAT3 | MA0144.2 | chr3:126690946-126690957 | CTTCCCAGAAG | - | 6.14 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61225 | chr3:126659718-126703478 | HBL1 |
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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 |
GH03I126971 | chr3 | 126690205 | 126691470 |
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Enhancer Sequence | GGAAAGTCTC TTGTATTTTC CTCCTAGTGG CTGCAGCAAA GGGTCAGGTA GGGACACCAC 60 ACCTGGGAAT GCACACAGAG GAAGGTGAAA CCAAGAAATA GATGCCTGGT GACATTATGG 120 GAGTCCCCGG ATTCAGCCCT GCCTGAAGCC AGACAGGGAA GCACATTGAT GAATGTCCCT 180 TGGGATGAAG CAAAGCCGGG TTTCAGCCAG CTTCCTCCGG TGCTGTCCTG CCCATGGTTT 240 ATGTCCGGTG TCTACTCTGA CTGGCTGTTA AACATATACA TATTTTTCAG TTTTTAAAGA 300 TGGAGTCACA CTGTGTTGTC CAGGCTGGAG TCAACCTCCT GAATTCAAGT GATCCTCCCC 360 CCTCAGCCTC CCAAGTAGCT GGGACTGCAG TCGCATGCCA CTGCACCTAG CTTTGGCTGT 420 TAAATGTTTA AATGTTTAAA TATTTTAAAC ATTTTGGTGT TTATTCCTTG AGCCCAAAAA 480 GCTCTGCCAT CTGGATGGGG TCTCCAGGCC ATGGGGCTTG GAGCTAGGTG CTGTGTGTTC 540 AGGTCCAGCT CCTCCCTTCG CTGCCCTGCT GCCCCCTCCT CAGTGGGCCT GCGTCCCTGG 600 GGCTGGTACC TGGCACACCA CGTGCCCAGG AAGGGTGGGC AACTCGGTTG GCCTGGGCTT 660 CTGAGGGCAC AGGAGAGCTG GGCTGGTTCT GCCTGCGCAT TTTCTGTGGA ATGCAGACCA 720 TGCTGGCAAC ACCAGGGCCT CGGGACACCT CTGCTTCTGA CGCAGGCCCA GGACAAGGGG 780 TGATGCCCTG TGGTGAGCTG CAGCTGCTCC CAACCCAGGC CGGGTGGGCG GGTGCTTCAA 840 GGCAGGCTTC CCAGAAGAGG AGGAGCCTGT GCGGGGGCTG GAGGAAGGTC AGCAGGGTGA 900 CCTCAGGGGA AATAAGTTGT TCCCTCTGTC TCCAGAACAG AGGAGCAGAA CAAGCATCAT 960 GTGCAAAGCT CGTGGTGAAC CGGGGAAAGC ACAAAGCACC CCCGTGATGG AGGGTGGGGG 1020 TAGGGTAGGA AGAGAGGCTG GCAGGGGGAG GGCGACTCTC TGCTTCCTCC GGGGGCCTCT 1080 GTGGCTCCGT CTGTGGCTGT CCAGAGCAGT TGCCAAGTAT GCCCCTGGGG CCTGTCACTT 1140 CTTCATGCCT TGGTTTCCTC ATCCATGTAA AGGGGGCAGT 1180
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