Tag | Content |
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EnhancerAtlas ID | HS055-08881 |
Organism | Homo sapiens |
Tissue/cell | FT33 |
Coordinate | chr9:133226960-133228310 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr9:133227548-133227559 | AATGAGTCACA | - | 6.62 | KLF16 | MA0741.1 | chr9:133228089-133228100 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr9:133228089-133228099 | GCCCCGCCCC | + | 6.02 | Nr2f6(var.2) | MA0728.1 | chr9:133227417-133227432 | TGAACTCCTGACCTC | - | 6.22 | Nr5a2 | MA0505.1 | chr9:133227409-133227424 | GCTGGCCTTGAACTC | - | 8.25 | RARA | MA0729.1 | chr9:133227414-133227432 | CCTTGAACTCCTGACCTC | - | 6.73 | SP1 | MA0079.4 | chr9:133228086-133228101 | GTGGCCCCGCCCCCA | + | 6.33 | SP4 | MA0685.1 | chr9:133228086-133228103 | GTGGCCCCGCCCCCACC | + | 6.57 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr9 | 133227579 | 133227879 | chr9 | 133228000 | 133228065 |
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| Number: 1 | ID | Chromosome | Start | End |
GH09I130351 | chr9 | 133227155 | 133228200 |
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Enhancer Sequence | CATGGTGAGC CCCCACGCCT TCTGGGACCC CGCCACAGGC TACTCAGGAA GCTTCCCACC 60 CAGCTGCCCG CTGCCTTAGA GGGAGAGTGA GGGCTGAAAT GGGGGACCTG GTGAGTGATC 120 CCTGAGTCCA AGAAAGCTGG GGGCTGGGGT CGGGGTTGGG GTCAGGGTCA GGGGATAGAG 180 GTTATCTGGC CCAGCATTTT CCAAATCCGT GGTTTCCATC CCAGCTCTAA AAATTTACTA 240 CTTATGTTTT TTTTTTGAGA TGAATTCTCT CTCTGTTGCC TAGGCTGGAG CGCAGTGGCA 300 CCATCTTGGC TCACTGCAAC CTCCCCCTCC CAGATTCAAG TGATTCTCTT GCCTCAGCCT 360 CCCGAGTAGC TGGGATTACA GGTGCCCACC ACCACACCCA GTTCATTTTT GTATTTTTAG 420 TAGAGGTGGG GTTTCACCAT GTTGGCCAGG CTGGCCTTGA ACTCCTGACC TCAAGTGATC 480 CTCCTGCCTT GGCCTCCCAA AGTGCTGGGA TTACAGGCGT GAGTCACTGT ACCTGGCCCA 540 AATTTACTAC TTCTGATACC ACTTGGAATT ATGATTTACT TTTCTTTAAA TGAGTCACAC 600 TTCCTTACAC TGAAACACAT TTATTTAAAT ATCCCTTATT CTTATAAAGG ATATTTAATA 660 TCGAAACTGT AAGCAGAAAA CCAGTTTCGC TTGGCTAAGG AAGCTGAAAA AACAAACACA 720 CCCCATAGAG CAATGTTGTA AATTCTCGAG GCGTGGACTC CGCAGAGGGC ACCCAGCCTG 780 CATCTGCACT CTCTGTGCTA AAAAGCGGAG AGTAGAAAGT GCTAGAAAGG TTAGGGACAT 840 GCATAGTAGC ACCAAACGGA GCCTTTCCTT GCTGTAACCC GGATAGAAGG AGATTTGGGA 900 GGGGCGTAAC CATTCCATTC TGAGATGCAG TTATTTCATG CTGTGCCCAT GTGCCCCTAG 960 CATTGTCCTG GGTAGCATCG GTGGTGAGTG ACCAGCCCTG TGTGAAGTCC TCATCTAGTC 1020 CAGCCTCTCA TTTCACAGAT GGGGAGACTG AGGCCCAGAG AGGGGAAGTG GCTCACCCCT 1080 GGTCTTCCAG TATGTTAGAG CAGAGCAGGG CCCAGAATCC AAGCCTGTGG CCCCGCCCCC 1140 ACCTCCTGCA CCTTCCACAC CAGCATGTCC CCATGCTGGC CTCTCCCATC TGTCCCCAGA 1200 CCCCTCCCCT CCTTGTCCAC CATGCCTTCC CTGCCCCCGC AATGGAAGCC TGTGGTGTGT 1260 CTTGTGGCCC AAAGGCATGA GTCTGCTGCC CTGGGGAAGA TGCCAGAGGC CTCAGCGGCT 1320 GCCTGTGACC AGCCCCACCT CTTTCCTTCT 1350
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