Tag | Content |
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EnhancerAtlas ID | HS184-23998 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr5:56052450-56053400 |
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) |
KLF4 | MA0039.3 | chr5:56053026-56053037 | CCACACCCTCC | + | 6.32 | STAT3 | MA0144.2 | chr5:56052818-56052829 | CTTCCCAGAAA | - | 6.02 | TFAP2A | MA0003.3 | chr5:56053136-56053147 | TGCCTGAGGCA | - | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_61799 | chr5:56021081-56060615 | Toledo |
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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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Enhancer Sequence | AGTCCCCCTT TTATAGATGA GTGAACCAAC ATGCAAAGAA GCTTACTAAC TAACCAAAAG 60 TCACTCAGAG AATGTGGTAA AGCCCGAATC CCAACCTGAA CAGTGAGCTC AAAAACCTCA 120 CTCCTAATCT TGTCTCCTCA GCCTCTGTGG AGGTTTGGGA CAACTAAGGA TGGAGGGATC 180 CCTCAGGTGA GGGAAGGTGG GGTGGGAAGT GGAATTTCCA GTGGGGAGGG GGTGGGGGAG 240 CATCTGAGGT GGATGAAGAG TGAGCAGTAG TCCTCCTCTT TCCTGTTCCT GAAGCAATAC 300 AGAACCTTAC AATAGCTTGC GTTGGAGTGT CTATGGGGGC TGAATGCTAG ATTTCGGGTC 360 ACTGGGCCCT TCCCAGAAAG AACAGTACCG TCTGAAGCGT GCCCCTCACT GCTAAGTGCT 420 GTAGATCCGT TGTGTCTTCA AGCCAGAGAT GGAGATGTCT GTGTTCAGTT GGTCACCTCA 480 TCCCGCACCT CCCTCTTCCT TCCCCTCACA GCCCTATCTC AAATCACTTC CCAGCAATGA 540 CTTGCCCTTC TCCCTCCAGG GCTGTCCCTG CATTCCCCAC ACCCTCCCGG CTGGCACCTC 600 TGCCCAGGCT GTGGTTTGGC CCCGGAGGTC TGGACTGGAC AGGGACAGCC TGAGCTGAAC 660 CTCAAGGAAC AGGAAAGTTC AGTGTTTGCC TGAGGCACAA CGAGTCATTC AGCAGTCACT 720 AACTCTCGCT CCTTAGCACT CCATCCCCCT GCAGAAACCT TCCCAGGGGA CATGGGGACA 780 TTTAGCCCTA TTGAAGAGAC TAGCCTCCAT TGGCCTACTT TCTTCCCTCA CACTTCCTTC 840 AAGGGGCTTT AGCAAGATTT ATTTCTGACA GAAATGTCTT TCTGTAGACT TGTAAATATT 900 CAGTCACTTC ACAAGTTTGC TTAAAACTGT ACCAAACTGT ATTTTATTCC 950
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