Tag | Content |
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EnhancerAtlas ID | HS092-19856 |
Organism | Homo sapiens |
Tissue/cell | HFF |
Coordinate | chr16:87027110-87029680 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
NFE2L1 | MA0089.2 | chr16:87028323-87028338 | ACAGCTGAGTCATTG | - | 6.31 | RREB1 | MA0073.1 | chr16:87027183-87027203 | CCCCCCACCACCCACCTCAG | + | 6.4 |
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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 |
GH16I086993 | chr16 | 87027518 | 87029163 |
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Enhancer Sequence | TGTGAGGCGG GGAGATTCAT CAGCAGCAAG GAGACAGACA GGACAGCCGC TGCCAGCTCA 60 CATCCACCCC CTACCCCCCA CCACCCACCT CAGCTGGCCT CGCCGCAGCC AGGCGGACCA 120 GTCCATGCAG GCTCCAGCCC CTCCGTGCTG GCTCATTGTG CCACAAGCAC AGGCCGCTGG 180 TCTCCAGTCC TTCCCAGAAC TTCTCCAGTG CCGTGAGGCT GAGGAAGCCC CTCGGGCCTT 240 CCACATCACC GCAGGGAAGT GGGGAGTCAG CGCTTGACCC ATGAAGGGAC GAGATCCATA 300 GATAAGTACT CCTTTTGGGC AGACAATTCT AGGAGGTGTT CTGTGCACGT CTTAGGAGGT 360 CACGGTGGGA CTGCACCCCG TGCCCCAGCA GCGACGTCAA TCGCACAGCC TGCTCCTCCT 420 GACTTGCCAC TGAACCCATG CGCCCTGGAC AACCTCCCAA GGAACCCACC ACTGCTCCAC 480 GGGCAAGTTG CCGGCTGCCT TTGGGGAGCC CAAGATAAGA GCAGGGGTGG ATTAGAAGGA 540 TGGTGGGGGA ACGAAAGCCA CGTGTGGGAC AAAAGACGAT CATGAAAGCT CGTCTAGACC 600 CAGGAAGGAA ACCTAAGTGT CCAGATGAAC ACCGCTCCAC AGAGAAGTGG CAGCAGAGCA 660 GCGGACGGCA GAAACCACGC CTTGCCGAGC TCCCACGGGG CCAGAATCTA CCCCACAATT 720 CGGCTTCATC TTAATCTACT AAGCCTCCCT GCAAAGACTT TTATCACTTC TTTGATTTTA 780 CAAATTTGGA AACTAAGGCT CAGAGAAGTG TGGTTTTACC TCTGAAACAC GCAACTTCCC 840 ACCCACCCAA AATGAGTGAT GGAGAAAGAA CCAACAGGAT TGGGCAACTG TTGGATGTTG 900 AGCAAGAGGG AGAGAAGAGT TGACTCGGAG GTTGGTATAC TCCAAGAAGG CTTCCTGGAG 960 GAAGTGGACA ATTCAGAACA CAGGACCCTT TATCCAAATC AAATACAAAT AGGGAACACT 1020 ATTATTAAGT ATTATCTCCT ATCTCTGTAA AAAGCCTTGT GGCCAGGGGG TGTTCTGGAA 1080 ATGCTAGTTA ATTTCTGGTT AAATATTGGA TCCCTGGGAG TTCTTTAAAG GCTCGTTTAC 1140 CCAGCCTGGA AGTTAAGCCT GTAACTTAAA CGCATTGTCA AAACCAGGAA ACATTTACCC 1200 CCCAGTCCAG ACCACAGCTG AGTCATTGGC CAGGAGAAGC TCAGTCTGTG TGCAGAGAGC 1260 TGGAGATTAT CTCATCTTCC AGGCACTTGT AGACATCCAA TCTGGACAAA TCATGTCCCA 1320 CTCCCAAGAA TCTGCAAGAA ATGGCCTGAT GTGTCTCCCA CAGAACAGCC GATGATGATA 1380 ACTCATTGTC ACTCGAGCCA GTGGGCAGAT AATGACCCCG CTGACAGGGT CCAGCCTGCT 1440 GCTCCGCCCC AGCAGACATG CTCCAACAAT GGCTTCATCA TCCTCCCCAC CGGGACTGTG 1500 TAGATGAGGG AGGTGCCTCC CGCGGTGCAG GCTGTGAGCT CTAAGCAGTC ACGCTGGACG 1560 CTGGACCAGT GCCCTGGGCT GCTCCTCCCT GCAGCCCCAC GAGCCCAGGT AGGGATCACC 1620 AGAGGTCGTT TCACTCCCAA GTGGAGTGAT AAGTCAGTCC TTCTACAGGA AGATTTCTCA 1680 CAAAGTGCCC TACTGCACTG TCAAAGGGTA AAAAGGAGAA AAAAAATAAT AAAGCCAGAG 1740 GCAAGGGCTC CAGGCAAGAG CAAGATGACA ATATTTGTAC AGCGGGGTTT GGAGAGGAGC 1800 CCCCGTGAGA GCCCAGCGTC TGAGAGAGCC AGTCCTTTGA ACTGTCCCAC CCTTTGTTAT 1860 GACAAGAGAC TTGATAAGCC CACCCAGCAC AGAGACCCTT AGAATCCAGG CATATGGACT 1920 CCATTAATCT GCCCTTGCAC CTTTTAAGTA CTTTGCAGCT CCTGCCGCCC ACAAAATCCA 1980 AGCAGAGTGA GAGTCGCAGG GTTAATTTTC TTAAATGGAT TTTAGTCAGG CAAGCCCCGG 2040 ATTTCTTTGG AGGGCAGAAG TTGACAGCTC ACTGCTGGCC CCAATCTGTC CTTGGGGTAA 2100 TGACGTCTGC CGCCCCTCAG CATGGGGACC AGATGCGGTC AAGGTGGTGG AAGCAGCAAG 2160 CAATGGGAAA GCCCAGCCAG CTTAGGCAAC CCAGCACGGG GGAAGGCAAG GCGGTGGCTG 2220 GGGGACCGCG CCCTGGGTTG CATCCCCGCG TACCACTGGC CGGCTGTGTG CAAGGTCAGA 2280 CACACACCTT AGATCCTGTG CCCGTTTCCC CTTCTGAAAT CAGAAGCCAC CATCGCTCCT 2340 CTGCCCTGCT GTGAGGAGGA TCGTGAGTTA CAATGTGTAA AGCGATGATA ACAGTTCATG 2400 CCATTAACAA GCGCTCAACC AAGATGTGCC GACTGGGTGA GGGAATGAGA AACAACAGCA 2460 ACCTTCAAAG CAAGAATGAG CATCAAGACA GCACGCGCCA CTGTGCTGAG AGCTTTAGAT 2520 GTGGTCTTTC CAGCCTTCCC AACCATCCTT CTTGAGATTC TAGGGGCTAG 2570
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