Tag | Content |
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EnhancerAtlas ID | HS043-01489 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr1:58085280-58087350 |
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) |
Esrra | MA0592.2 | chr1:58086792-58086803 | ATGACCTTGAA | - | 6.62 | Esrrg | MA0643.1 | chr1:58086792-58086802 | ATGACCTTGA | - | 6.02 | Myog | MA0500.1 | chr1:58086442-58086453 | AACAGCTGCAG | + | 6.02 | Nr5a2 | MA0505.1 | chr1:58086791-58086806 | CATGACCTTGAACTT | - | 7.55 | SREBF2 | MA0596.1 | chr1:58085984-58085994 | ATGGGGTGAT | + | 6.02 | Tcf12 | MA0521.1 | chr1:58086442-58086453 | AACAGCTGCAG | + | 6.62 |
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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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Enhancer Sequence | CCAGGCTGGT CTTGAACTCC TGGGCTCAAG TGTTTCTCCC CGCTTGGCCT CCCACGGTGC 60 TATGATTACA GACATGAGTC AGGGCCCCTA TTTTATAGAT AAAGAATTGG AGCTTTAGAG 120 AGATGGAGTT GGCCAAGAGT GTCCTATGAA ATATTTTAGG GCCAGCAGGG ACAATCCTTC 180 TTTGTCCAAC TGCCAAGCTT CATCCTGGGA AAATGGAGGT CAGGGAGGAC TTCAAGGAGG 240 GGAGGGGTCA ACTGGATCCA GAGCAGAGTG GGACTCTGAC CAAGGGCTGA GCAGGCATGA 300 ATACCACCTG AGACGCAGAA CAGGACAGCA AGGCTGCTAG AGACTGTCAA GGCACAGAAA 360 GACTGAGCTG GTGACAAGAA CAACGACTGG AGACATTTGA CACATCCCAG AATCCTCGCC 420 TTTACTGTAT TTGTTACTTC GTTACTATCT GCCTGCTTCC AACAGGGATC CATGGTCATT 480 CCCTCCAGAG CAGGCTTGCG GGCTTGTTTT CAGGGGTAGC AAAAATGGCA ATCCTGGAGA 540 ATTTGTTTCT CTGGTGCCAG CTGAGACTCC GCCCCGAAAG GAGAACCTCC CAGTAGAGGA 600 GCTCAGTGCG AGAAGGGGTC TGGGCTTTCC ACAGGAAAAT TTCACACAAG GCCAAGCAGA 660 TGATGAGTTT GGATGTCCTA ACCTATTCTC TTACATAGGT ACATATGGGG TGATGGGGAA 720 GATTCCTTTA CTCAACCAAT GTTTACAGGG TTAAACGAGA ATGATAGGTC CCTCTGGACT 780 TGTTTCCAGG ACTCCAGGGA AAATGCTAGT TTTGTATGAG ATGAATCTCA AAAAATGCTT 840 ATTAAACAGA TGACTGACTG GTAATTGAGT GAACTTGACT TTTGAAATAT GTACAGAAAT 900 AGAGTGTTTC CCATGAGGGG ATAAACCCGC AGATACAACT ATCAGCAAAA CCTGGGGTGA 960 GAGTGAAGGG AAGGGGTTGG ATTAAAGAGG GCTTTGAGAT AAGAGGTACC CAACATGTGG 1020 CACAGTGCCA GGCACCCAGA CACCTAAAAG ATGTGCTGCC TGTCCTCATG CTTTCCTTCT 1080 CAGGCCAGCA GCAGCAGGAG TAGGGGAGAG AACACAGATG CAGAGAGGGA GAGCTAGACA 1140 GGAGGAGGTA GGAGGAGGAC GTAACAGCTG CAGTGTCACA GGCTCTGGGT CTGGAAGCAG 1200 GGGGGCAGCG CGGCAGACAC ACCTACTGCC CTAAATCATT AGCAGCAACA GCACGCAGAG 1260 CTTTGTTTGT GTTGCCTTCT GCTCCAGATT GTTGCTTCCT CACTGACAAG ACAATTTGCA 1320 GACTGGCCTA CTTTCTCATG CCCACCTTCT GCCTTGGGTT CAAAGAGTTG GTCACAAGGG 1380 GTGTGTGTGT GTGTTTGTGT CTGGGTGTGT GTGTGTGTGT GAGAGAGAGA GAGACAGAAT 1440 TCACAAGGTT AAGCTTGTGT GCCTGTTTGT CTGAGAATGT GTTTGTGTGC ATAAGACTGA 1500 GAGACAGAAT TCATGACCTT GAACTTGTGT GTATTGGGGG AGACAACAGA ATTCATAAGC 1560 TTGAGTGTGT GTGTGTGTAT GTGTGTGTGC ACATGCACGT GTGTGAGAGA ATTCATGAGC 1620 TTGAGTTTGC GTTTAAGAGA GGGAGTGAGA TTGTTGTGTG TGTGTGTGTG CGTGTGTAGG 1680 AGCCCTGAGA TGGGGGAGAG TTGGCCTGAA AATGATAAAA GGCCTTCCTT TTACTCAGTA 1740 ATTTTACTGC TTTTGTGAGG GAATAACAAG CTGGGATAGT GCGTGGGGGT GGGGAAGAGG 1800 GCGCAGAACT CATGAACCCT CACTGAAGGG CTCTCCTACC CTCTATCTTT ACTTCTGTAC 1860 TTTTGAACAA TGCTGGGGCT TACTCAGGAT TTCCAGTTTC TGCAGGGTTT GGGGGAAACT 1920 GAGGTTGTCC CTAAGAGGGT TTAGGCTGGG GACTCTGAGG CTAGGCGATT GTAAGTTCCT 1980 CCGTGGAAAG GTGCACACAT GATCCCTCAC ACCTGCGCCT CTGGATCTGG CATGTGATCC 2040 AGCACTAGCA GGTGCTCAGT AAATGTTGTT 2070
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