Tag | Content |
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EnhancerAtlas ID | HS012-03787 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:48186070-48187490 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr11:48186639-48186650 | TCTGACTCATT | + | 6.32 | HSF1 | MA0486.2 | chr11:48187149-48187162 | GAATGTTCTAGAT | - | 6.03 |
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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: 2 | ID | Chromosome | Start | End |
GH11I048164 | chr11 | 48185727 | 48187103 | GH11I048165 | chr11 | 48187121 | 48187270 |
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Enhancer Sequence | AGGCCAAGAT CTGTATTTGA CATTCCACCC TTCCCCTCCA TTTTTTTTTT TTTTTTTTTT 60 TTTTTTGAGA CGGAGTCTTG CTCTGTCGCC CAGGCTGGAG TGCAGTGGCA TGATCTTGGC 120 TCACTGCAAC CTCTGCCTCC TGGGTTCAAG TGATTCTCCT GCCTCTGCCT CCCAAGTAGC 180 TGGGATTACA GGCACGCACA CCATGCCCAG CTAATTTTTG TAATTTTAGT AGAGACGGTG 240 TTTCTCCATG TTGGCCAGGC TGGTCTCGAA CTCCTGACCT CAAGTGATCT GCCTGCCTCA 300 GTGTCCCGAA GTGCTGGGAT TACAGGCATG AGCCACTTTG CCTGGCCCTT CCCCTCCATT 360 TTTAAAAGGT TGCATTGTGT CATGCACTTG TGTTAAAATA TGTCACCCTT CCAGATCTTT 420 CCAGCTCTTG GCTGTGAACT AACACTGGAT TTCTTTGCAG ACTTTAAGCT GACTTGGAAT 480 TAAATTACCC AATACAAGTG ACATAGTAGT ACTGATGTCA GTAATGGAAC TACTACTGAG 540 ATAGTGTCAG GATTCTTTAC CTTGCTGCCT CTGACTCATT AAATAATCTT AGGACATCTT 600 TGAACTTTGG CTTCCAGGTT TTAAACTCAT AAAACTGGTA TTTTCCAGTC TTTGTTTCTA 660 AGAAGGTCTG ACCATCTTTA AAATAAGCTA ATGAAACAAA CTCATCAAAC ATTAATGATG 720 TGACATATCA TAATGCTGCT TAAATGTTAA TACAGCAATT TATCCTCACC CAGACTTGTA 780 CATTTTAAAG ACTATCAATT ATCATAGCTA CAGAAGGGTG GCTGACCAGC GGAGAAAAGG 840 AACACTTAAT ATCTATGGTA TAGTTTCTGT ACTACTGCTG GATTTGGTTT TACCCAAACT 900 GTTACTGAGA AGTGTTTTTG AGGCATGTTT TCAACAGAAC ATATTGCAAA GTTGCTTTCC 960 TCAAAGGGGT GAATGTTCCT TGACCAGGAT GAGAGCAGAA TATTAATTTT GTATCAGGCT 1020 ATCGTCCTGT ACCGATTTAG AACTCTATGA ATATGTGCTG TGTTTTTGAG TCTAGCAGGG 1080 AATGTTCTAG ATGCCTGGGT ACATTGCGTG CTCTGGGGTG AGCTTGGTGG TTGTTGTGGA 1140 AAGAGTGAAA TTCAACTCCT GTGTTGGTCA AAAGAGAGAT TTTCTTTTTT CTGCTATAAT 1200 TATATAAAGT AGTATTTCTC AATCTTTTAT CCTTTTTTGA GAAACATAGA ACTCTTATCC 1260 CTGCTACTAG AGTCTAATCT CTTTTTTATA TTTTGAAAAC AATACTTATT CATATGAAAG 1320 CATTTGACAA TATATTTTTC TCTCCTCTTT TTTTTTTTTT TGAGACGGAG ACTTGCTCTG 1380 TCACCGGGCT GGATTGCAGT GGTGCGATCT CGGCTCACTG 1420
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