Tag | Content |
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EnhancerAtlas ID | HS092-02081 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr1:67821180-67822510 |
Target genes | |
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) |
Gata4 | MA0482.1 | chr1:67821902-67821913 | GAGAGATAAGA | - | 6.32 | PLAG1 | MA0163.1 | chr1:67821273-67821287 | GGGGCCCAAGGAGG | + | 6.39 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr1 | 67821585 | 67822244 | chr1 | 67821491 | 67822210 |
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| Number: 1 | ID | Chromosome | Start | End |
GH01I067355 | chr1 | 67820960 | 67822697 |
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Enhancer Sequence | ATCCAGCCCT TCTACTCAAG ACCTCTTGAA ACTACAGGAA GAGTCAGAAG CCAGTATGGT 60 CATAAACACA GGCTCACAGA GATGGCAGAG ACTGGGGCCC AAGGAGGTGA AGTAACTGAG 120 CCAAGATCAT ACATCCAATA GTGGCAGAGC TACATGGAAA ACCAGACCAC CCTTGGGTGA 180 GCACTTTTTC CAAATGCCTT CTGAACGTTA TAACTTCATA CAGAAGCTCT CAGTGAAAAT 240 GGAGATGGGA AGTTGAATGA TTGAGGCTAA AGGAATAATT TTGAAAGGTG ACAGGGAGAA 300 GGTGAGTTGT TAGCAGACTT TTGAAGGAAA GAACATGCCC CAGCAAACAT CATGAGAGAG 360 GAAATTCTAG GTTGGTTCCT GGCAAGTGTG GTGACTCAGA GACAGAAGAA CCCTAGGCAA 420 TGCCAAGTTG ATTTACTTAG CTAATTCCAG AGAAAGTAGT GGTTAGAAAG GCTCTTTGGC 480 TTTTTTACCT CAATACTTGG CAAAGGATCT CGCAAACCAT AGTGTTCAAT AAATACTTGC 540 TGAATGAGTA AATTTTATTC TCAAAAAACA AAACAAAATA AAAAGCCCAC AGTATAACTG 600 GGACATCAAA TACCAAGGCA AGTGAAGACA AGGAACCATT GCTGGGAATT CCAGTTCCTG 660 ACAAGATGTC CAGTACACTG TCTACAGGCT CTACCACTAA ACCTGGCCCT GAAGCTGCTG 720 CAGAGAGATA AGATATGGAT GGCTGAGTTC CCCCTCTGGG GAATAGTGAT GAAGCGGGGA 780 GGACCAAGGG AGCTTTCTAC TTGTTCTCTT TGTTTTTTCC TCTTGTTATC CTGTTGTGAT 840 CGCTGCCCAG GAATCTCTAT GATGGGGTAG GAAATTCTGG GGAGCAGTGC AGAGTCACTG 900 TCAAGGCAGC CCTGGAACCT CACTGGGGAG GAGAGCTGGG AGCAAAGAGT GCCTGTGAGC 960 TGGCTGACCC TTCAGCATTT TTTTCCTGCC ACCCATCCCA TGGGCCTGGC AGTTTCAAAC 1020 AAGAATAATA GCTCAATTCC CTCACGAAAA GCAGTGCCTA CCACAGAGGT ACTAGTTTGA 1080 TTCTGGAGGT ACAAGTATGC CTAAGGGGTG CCTGGGGACA AAGAGCTCAG CTTGTATCAC 1140 TGCAGGGTCT CTGGCCTGGA GCTTTCCAAG CTGAAAAGCC CTCCTCTCTA CCCTAAACAT 1200 ACATGGAGGA CCATGAGCTA TAGCTGTACT TTGACTCCTC TCCCTATAAA AAAAGAAAAG 1260 CCAAGGTTGT TGACCAATCA AAGAAAATAA AACATGATCC CAAAAGAAAA CATCAAGACA 1320 AATGTGAAGA 1330
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