Tag | Content |
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EnhancerAtlas ID | HS012-04338 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:70058080-70059350 |
Target genes | |
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) |
BCL6B | MA0731.1 | chr11:70058567-70058584 | TGAGTTCCTTGCAAGCA | - | 6 | IRF1 | MA0050.2 | chr11:70058634-70058655 | TTCAGCTTTCACTTTTGGTTG | + | 6.32 | ZNF263 | MA0528.1 | chr11:70058260-70058281 | CACCCCCTCCCACCCTCCCCC | - | 6.14 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr11 | 70058304 | 70059000 | chr11 | 70058385 | 70058983 |
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| Number: 1 | ID | Chromosome | Start | End |
GH11I070212 | chr11 | 70058144 | 70059155 |
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Enhancer Sequence | ATCTCCTGAC CTCATGATCC ACCCACCTCG GCCTCCCAAA GTGCTGGGAT TACAGGAGTG 60 AGCCACCGCG CCTGCCCAGG ATGAAATCTT AATCCATGCA TCATCATGCA TGGGACGGGG 120 TACACAACTG TGCAGAGCCC AGCCCAGTGC CATGTTCCCT CCACAGCAAG ACTGTCACCT 180 CACCCCCTCC CACCCTCCCC CGCAGCCCTT GCCCCTGCTG TTTCCTCTCC CTGCAGCCTT 240 CCTCACTATC CACCCCAAGC CCCCCAGCTC AGAAGACATC CTTCTGATGC AGGCTTGCCC 300 ATGCACCCAC TCACAGTGGG ATCCCTGCAG CCCCCACTCC TGCCCGGGTC CTGCTTCCTC 360 TAGCGCGACT CCCTGAGGGC TGCTTCCAGC ACTTTCCAGC GGCTTCTGAG TGAAGGCTTA 420 TTTTGTGTTT GCTGAGTGAA TGAGTAAACA GCAGCGATCA AAGGCCCACT AGCGTCTCTC 480 AGGGGCCTGA GTTCCTTGCA AGCAGGAAAG CAAAAGATGC CTCCGCCCCA GGGTTTCAGA 540 TTCCTGGATT CCCCTTCAGC TTTCACTTTT GGTTGGGCTT CCCAGCCCAG TCAGTCGGAC 600 TGTGAAAGCA CCTGCCCCGC AGTAGGCACG GGCAGGGCAA GAGGGCATCT TCTCAGGGGA 660 GCCAGGTATG CCCCTTGGTC TGCCACCCAT GCATCATATG CCCCTGTTCC CTGAGCCTCT 720 GCTCCCCGCC CCTGGTCCAC ATACCCCCGC CCCGGTGCCC TTCACTCTGA CCAGGCCCAG 780 TGAGCTCCAG CCAGGAACCC CAGGGAGGAG TCCCCACCAC CTGAGTCACT GCAGGCCATC 840 CCAGGGGTCC TACTCGCCAG GAAGGGTTGA CGCCCACGTA CACATACACC TCTGGGCTCC 900 TGGCACTCTG AGCTGTATGT TTCATTCTGG TTCATTCACC ATTCATTCAT TTACTCGGTA 960 GATTCTTAGC AAAGGGCTAC CAGCTCAGAC CGGGAGTGGC CAGCTCTTCT CCCTCACCAA 1020 TGCTCCCTCT CCCAGCAATG TTGTAAGGTT CAATGAGATG TGGTGTGGCG AGGTCTGGGG 1080 GTGACAGCCC AGGATAAACG TCACTAAATG TCATCATTGT TACTATTCTT AAGGAACTGC 1140 CTGTTTTAAA ACAAGCAGCC TTAAAATTAA AGTGTAGGTA TGGGGCCAGG CACAGTGGCT 1200 TACACCTGTA ATCCCAGTAC TTTGAGATGC CAAGGTCGGC ATTTCACCTG AGGTCAGGAA 1260 TTCAAGACCA 1270
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