Tag | Content |
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EnhancerAtlas ID | HS139-51202 |
Organism | Homo sapiens |
Tissue/cell | Myotube |
Coordinate | chr7:97894370-97895860 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr7:97894371-97894383 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr7:97894371-97894383 | TCTATTTTTAGT | - | 6.32 |
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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 |
GH07I098265 | chr7 | 97894656 | 97896185 |
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Enhancer Sequence | CTCTATTTTT AGTAAAGATG GGGTTTTACC ATGTTCCCCA GGCTGGTCTC GAACTCCTGA 60 ACTGAAGCTA TCTGCTTGCT TTGGCCTCCC AAAGTGCTGG GATTACAGCC ATGAGCCACC 120 ACGCCCGGCC AGGATTACAT TTTCCATACG AGCCCAGTGT ATACATTACA GCAATTTTAT 180 TGGTGTAGTT TCAGGGAAGA TAATTTATTA CTCCCTCTGT AGGGATCGTA ATCTGTGAGG 240 GTCTTATCTC TGGCTCTGTT TAGTCTTCCT AATTATTTAT TTATTAAAAA CAATTTTATA 300 GAGACAGGGT CTCACTATGT TGCCCTGGCT GGTCTGGAAC TCCTGGGCTC TAGCCATTGT 360 CCTGCCTCAG CCTCCCAAAG CAGTGGGTAT AGGCATGAGC CACCACACCC AGCCTAGTCG 420 TCCTAATTAT TTACAGAAAA AAAAAAAGGC AGAAGTTGCC AGGCACGGTG GCTCATGCCT 480 ATAATTCCAA CACTTTGGGA GTCCGAGGCG GGTGGATCAC AAGGTCGGGA GTGCGAGACC 540 AGCCTGGCCA ACATGGTGAA ACCCCGTCTT TACTAAAAAT ACAAAAATTA GCTGGGCATG 600 GTGGTGGGCG CCTGTAATCC CAGCTACTTG GGAGGCTGAG GCAGGAGAAT CACTTGAACC 660 CGGGGGGCGG AGGTTGCAGT GAGCCGAGAT TGTGCCACTG CACTCTAGCC TGGGCAACAG 720 AGCAAGACTC TGTCTCAAAA AAAAAAAAAA AGCTGTATGC CATGTGTGAG TCAAGCCACC 780 TAGCCACATT CCTCTCAAGG GTCAGAATAA TTTAAAATTC CAACAGCTGT AAATTTGAAT 840 TCTTTCACGT ACTGAACTGT CAAAAACCCA GTCATTGTCC CTTCGAGCTC ATCAGCTCAG 900 CAGCAGGGCT GGGATGGATG CCTGGGATGA CATGAATTCC TCCTGTTCCT TCTGTCTTTC 960 TTTAAACAAG TCACCAGGGG CCATATCCAT GTCCCATGGT GGGTAAATGG TGTTGTGTCC 1020 CTACAGGCCT CCCGCTCAAG GCTCTCTCTG GCCAGGAATG TGGATTTCTT AATGCACAGT 1080 TTGACCAGCT CCTTCACTGC CAGGCATAGA TCTTTAGGTA CTGTAAGTGT TCAGTAAGCA 1140 CCCGTGAAAG GTCAGAGATG GGGGCAGACG GTGGAAGTGA TTCAGAGAAA CAAGAAGGAG 1200 AATTTGATTG TGGTATGAAA AGGCTTCCAC AAGCAGCCAA AGATAAAATA TGCCTATTGA 1260 TCTACAGGAT GTCAAATTAA GAAAAACGGC CAGGTGTGGT GGCTCACGCC TGTAATCCCA 1320 GCACTATGGG AGGCTGAGAT GGGCGGATCA CAAGGTCAGG AGATCGAGAC TGTCCTGGCT 1380 AACACGGTGA AACCCCATCT CTACTAAAAA TACAAAAAAT TAGCCAGGCG TGGTGGCGGG 1440 CGCCTATAGT CCCAGCTACT CGGGAGGCTG AGGCAGGAGA ATGGCGTGAA 1490
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