Tag | Content |
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EnhancerAtlas ID | HS044-05267 |
Organism | Homo sapiens |
Tissue/cell | Fetal_kidney |
Coordinate | chr16:57546780-57548260 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Esrra | MA0592.2 | chr16:57547085-57547096 | CTCAAGGTCAT | + | 6.02 | Esrrg | MA0643.1 | chr16:57547086-57547096 | TCAAGGTCAT | + | 6.02 |
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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 |
GH16I057512 | chr16 | 57546769 | 57549553 |
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Enhancer Sequence | GCCTGTGGGG TGGGGGTGAC AGGAGGTTAG AGCAGCCTGG CTGGTAGTCC CCCGATAAGG 60 TGGCTGCAGC TGGTGCTGGA GCAGTTAAGC CTTCCCTGGT GCTTTCCCTG CTGTCTCATC 120 TCCTGTAATC TCCTTATATG ATAGAAGTGC CATTATCACC CCCATTTTAC AAGCAAGGAA 180 ACCGAGGCAC AGAAAGGTGA AGTCATTTGC TCAAAGTCAC ACAGATGGTG GGGAGTGGGG 240 CAGAGCTCTG AACTGAAGTG GGTGGTGCCA GAGCAGCTGG GCGGTTAGAG AGGTGAAGGA 300 GCTGGCTCAA GGTCATGCTG CAGGATTTGA ACCCAAGCCT GGCTCTCAGA GCACAGGCAG 360 CAGAGTTGGT TGGTGTGACA GTGCAGGGTG GGCTGAGCCC TCTACATTCC CAGTGTCAGT 420 GAGAAAGGGC TCAGCCCTAG TTCTTCCTCA CATTAAAATT CCTAAAGTCA AAATTTACGA 480 GGAAAACTTT GAGTCTAAGA AGAGCTGGTG AAGGAAATGC CGATCCCTCC CCCAACCCCC 540 CAGCAAAGTG GCCGCCCCGG CTGCATCTTA CTGGAAGACA TGAATTATTA ACACGTAAGG 600 GAGGGGCACA GGCGGGGGCC TCCATTACTG CACAGTGATT TAGTGAGCTG TCCCCGGAAC 660 ATTAAAGCAC AAAAAGTTGG AAAATAAAAC GACACAGCGG TCCTGGGTGG CCCCACCCTC 720 CCCGATGGAA GCACTTGAGA GGCCCAGCAG GGCCTGCCTG CCCACTTCTG GAGTTTATGG 780 CTCCTGAACA ATGTGACCCA GACTGCGGGA AAGCCCCAAG GCTAAGTGGT CTTTTGAAGG 840 GTGTGTGCTG CAGGGTCAGA GCAGGCAGAG CCAGCCAGGC ATGGGTCCTG ACTTGGGCCC 900 ACGCCTGGGC CCCTGCACAA CACTTTATGG GCGTCATCCC AGGCAGATGG GGAAATCGAG 960 GCTCAGTTTA CCATGGCACA ATAGCTGTTA GGTCTCTGCA GCCCATTCTC TAAGCCACAA 1020 GATCTCAGCA AACAGCAGCA TATAGTAAAT GCTCAATAAA TAAGGGCTTG GATGGCTGAT 1080 GGCCAGGGGT GATTCTGCCT GGCCACCCAC CAACTGTGTG GCCATGGAAA GACTTACCCT 1140 CTTGGGCCTT AGTTTCCTCA TCTGCCAGCC CCCTAGGAAA AAACATCTTT CCTTTCTCTC 1200 ATAGAAGCAG CGTGATGCTG ATGCACAACA TGTAACCCAA ATATAAGCCC CTCCGCAGCG 1260 GTAGTAGTAA CAGTAGTAAT AGCAGCAGCT GCTGACAATC ACTCAGCATT TATTATGTGC 1320 CAGGTGTTTT CTTTCTTTTT TTCTTAGAGA CGGGATCTCA CTTTGTCTCC CAGGCTGGAG 1380 TACCGTGGTG TGATCACAGC TCACTACTAT AGCTATGAAC TCCTGAGCTC AAGTGATCCT 1440 CCTGCCTCGG TCTCCCAAGT AGCTGGAACT ACAGGCACAC 1480
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