Tag | Content |
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EnhancerAtlas ID | HS179-02966 |
Organism | Homo sapiens |
Tissue/cell | SkMC |
Coordinate | chr1:203517680-203518870 |
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) |
HNF4G | MA0484.1 | chr1:203518727-203518742 | ACAGGACAAAGGCCA | + | 6.03 | RREB1 | MA0073.1 | chr1:203518607-203518627 | GGGGTGGGGGTGGGGTGGAG | - | 6.62 |
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| Number of super-enhancer constituents: 5 | ID | Coordinate | Tissue/cell |
SE_00433 | chr1:203513781-203518813 | Adipose_Nuclei | SE_40925 | chr1:203517827-203518906 | Left_Ventricle | SE_46073 | chr1:203517538-203518872 | Osteoblasts | SE_55853 | chr1:203516457-203518914 | u87 | SE_67709 | chr1:203516457-203518914 | u87 |
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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 |
GH01I203549 | chr1 | 203518348 | 203519397 |
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Enhancer Sequence | AAAAAAAAAA AAAAAGGAAT TTTAAATGAG ATAACATATT TGCATCTCGT AGCATAACAG 60 TTGACACATC ATTAATGAGA GAGAGAAGTG ATATGGAATT TATTTTTAGG TCAACATGTC 120 AGTAAATGAT CAGGTTATTA TTCAAGGAAC AGAAGACAAG AAGACACACT CCCTAGGAAG 180 TCCCAGCAAG AATATTCATG CAGGTAAGAT AGCTGTGAGG AAACATTTCT ACAAATCACA 240 ACTGTCCTGT CCACCCATTG TGCTATCAAA ATTTCCGTTC AGAGAGAGAC TTTCCTTATC 300 ATTGTTAGAA AAATCAGCAT GCAAATGTGA TGAGCATAGA AGAAACAAAG CTGGTGAAAT 360 AAACACATGC GATAAAAGGA CAGAGAAAGC AGAATAAATG TAGGAAAGAA TCTAATTCTC 420 CAGAACTTCA GAGCCAAAAG GGGCCTCGGG GATCAGCTGA CAAACCCCTT AGTAACAGAA 480 CCTTCCCAGC AGCCTTTATT TCCCCACATC TCTCTTACAT TTTGCCAAAG ATAATATTCA 540 CTTTGATGTT GCAAAAGCTT TAGTTTGCTT GTTGTGTTTC CTCTCTCCAT AATGGTATGT 600 TAGGCCATCC TTTTGTATTG GCAAATTGGT CTGACAAAAA GAGCATTATA AATTGTGAAA 660 ATACAAACAA ATTCTCCCAG CTCTGAAATT CTCCTTGGAC TTCAGTGGTT GACACAAATA 720 ATTTAGAGGT GATGGAGTTC CTTGAGTGCA GAGGGTGACA GAAGTTCATT CTTCCTCTGG 780 CAAAGAGAGA GAGAGAGAGC TGTCTCCCTG CAGTTTGGGA GACTGGGCAA CCACTCTCTA 840 GGGATGCTAC AGAGCTTGCT GTCCTCCCTC CTTCCAGACA GGTTGGCAGT CCTGCTGAAA 900 GCTGACTCCT CTTTCCTGAA AGTCTATGGG GTGGGGGTGG GGTGGAGGAG TGCTATGCAT 960 CCAGGTGCCC CGCTCTGGTG TAACCTGAGA CTAGAAGGCA ACTATATTCC AGGCTTTTGA 1020 GAATACTGAG TCAGGGTAAT GGGGATGACA GGACAAAGGC CAGGCAGGAC ATGCTGGAAT 1080 TTGTTTTTGT TTTGTTTTGT TTTTTGAGAC AGAGTTTCAC TCTTGTTGCC CAGGCTGGAG 1140 TGCAGTGGCG CTATCTCAGC TCACTGCAAC CTCCACCTCC CGGGTTCAAG 1190
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