Tag | Content |
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EnhancerAtlas ID | HS045-62500 |
Organism | Homo sapiens |
Tissue/cell | Fetal_lung |
Coordinate | chr7:50789380-50790480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Nkx2-5(var.2) | MA0503.1 | chr7:50790261-50790272 | AAGCACTCAAG | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_41576 | chr7:50788917-50790596 | LNCaP |
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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 |
GH07I050722 | chr7 | 50789441 | 50792736 |
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Enhancer Sequence | GTCACCCATT CCCCACTGGG TAGGGGCCAA ACAGAAGGGT GATAGGTCTC CACTCTGTCC 60 TCAAGCAGAA TCTGGGGTGG CTGAGGATGG GGGAGGACAG ACGACAGCAT AAGGAGGGGT 120 CAGGCAGAGG GAGGCCCAGG ACTGGCTGCA GGAATGCAAG AGAAGGCTCC ATGGGGGTGT 180 GGCAGGGACT GCTGTGGGAA GGGAAGGTGT CTGGGCTGAA GTCCAGGGAA ATGGCCCAGG 240 CCAAGAAACG GAAGAAGAAG ACAGCGCGTG GAGCGGGGAG AAGGGAGCAG AGCAGTTCAG 300 TATTACTGGT GGCAAAGGAG AGCCCAGGCT GCTGGTAGGG AGGATCAGGC CAAAGACAGG 360 CTGAGGAGGC TGGCCCGGTC ACTATGCTAC CTCCTATGCC CTCCTCTCCT GTCTCTCCTG 420 CACCCCAGAG GCAGGGTGTA CCACGGGCCC AGTAGCTCCC AGCTTCCCAG GCTGTCCCCC 480 ACCAGCTGAG CCCCGAACCC TTAACCTGCA CCACGCCACA GCCCCTCTGC CCTGCCCACT 540 CTCATGCCCA CTCAGGAGGC CAAGGACTGG CCATAAACTT ACGTTCAAGG ACTTCCTGCA 600 AGGGTCATTC CAAGATCCAA AGCGGCTTCC TAAGGTGATA GAAAGGTCCC CTGGAAGGCC 660 CCAGGGTAAC CCCGCCTGGC ACCAAAGAAG TGTCAGGGCA AAGATGTTGG ATGGCACAGA 720 CAGAGCAGCT CTGAGAGCAT CTGTAGTCCC ATGAGCTTGC AGCAAGGTGG GAAATTCCAT 780 GTGTTCGAAG ATTTCAAAGC CACAGAAAGC ACATTCCCAT CTGCCAGGAG AACATAGTTG 840 ATGGGGGCAC ATGGGCAGCA ACAGCTTCAA AGCCCTGTGA CAAGCACTCA AGAAAGGGGA 900 GTCCAGGGTG AAGAGGTGAC AGAACCAGTG ATGCGAGCCA GGGTGACAGG GCCCAGAGTG 960 ACCGGATGAT GGGGGATGGA CTATGGGGGA GAATGCCAGG GTGACAAGGT GACAGAGTGA 1020 TGAGGTGGGG TGACAGGGTA CCGCCCCCTC TCCTTCCCCG ACATTACTTA TACCTGGCCT 1080 CCAAACACAC AGCTTGTTCT 1100
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