Tag | Content |
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EnhancerAtlas ID | HS012-03868 | Organism | Homo sapiens | Tissue/cell | Caco-2 | Coordinate | chr11:57909010-57910770 | SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
| TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Sox3 | MA0514.1 | chr11:57909752-57909762 | CCTTTGTTTT | + | 6.02 |
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | TGAACCAGCC TTGCATCCCA GGGATGAGGC CCACTTGATC ATGGTGGATA AGCTTTTTGA 60 TGTGCTGCTG GATTCGGTTT GCCAGTGTTT TATTGAGGAT TTTTGCATCA ATGTTCGTCA 120 GGGATGTGCA GCTGTTATTG TCAGTGTCTA GATGTTGACG CTGAGACTTG AGGTCAAGTA 180 ACTTGTACAA GGTCACACAA ATAGAAATGC CTGAGTGTGA GTTTGGAACA AACTCTGTCT 240 TCTGTGCCCA TTTTCTTAGC CACTATATAT ATTTGTGGGA TTCCAGCCTT ACCTTTGTGC 300 TGGGTGATCT TAGGTTGATT ATTGAGCCTC TAGTATCTTA AGGACTTCTC TCTGTTATCA 360 GAAGGCTAAC ACTTCTGAAC AATGTTGCCT GGAACATGTC TCCCAAAGAC CTGAAAACCT 420 CCATATGTTT TGTAATCAGA GAAGGGTGGT CCATTGCTGG CAATTTATGT CTTTATTTTC 480 TATTAGTTGT GGCCAAATGA TGTATGCAAG TACATATGTA CAGTTACCTG ATTCCCAGAA 540 TTTCTGCTGA AATGTCACCT TTTCAGTGAG TCTTTTTGAT GGTCTTAATA TCCTTATCCT 600 TACTTTGATA CTTTTAATTC CTCATACTCT GCAGCATTTT TTTCACAGCA CTTACCAACT 660 TCCATCATGG TAGAAGAATA TATTTCTTCT TTTTTGAACA TATATATGCC AGGCTCCACG 720 AGAATGAGCA TGAAGGCAGG ACCCTTTGTT TTGTTCCAAG CAACTAGAAA AGTGCCTGCT 780 ACATAGTAAG TTCTCAGTAG ATTCTTATTA AATAAATAGA TGAATATAGC CTCTTTTTCC 840 CTTTGGCCAG GATGATTTAC AGGAACTCCT TTTAAGAACA TGGCGAATCA TTGTTCTGGG 900 AGAAGATCAG GGTAAGATTT GGCCTTAAGT ATAGAAAAAC AACCTAAATA TTTACCCTAT 960 CAAGAATTCA GTGGGGGAAA AAACTCCCCC CAGTTGCTGA ACATTATTCA AAAATTAGAT 1020 CAGCTTTTGC CAAACATTGA TCAAGGTTTT ACTTTATTCT TTATCTAAAG TCCTATGAGA 1080 TCTTTTTCAA ATTCAGTTTT TGTTTCAAGG ATGGAAAGAG GACAAGAAGA ATCACCTCTG 1140 AAGTCCACAT TCACTATGTT CATTACTCTA AATTATCAAG ATTCAAAGGC ACAGAGATAG 1200 TATTTTCCCA ATACCTGGCG AGAACCCCAT CTGTATTAGA ATTCAAAACT CAGTGTGCTG 1260 GCTTTGTCTG TTAATGAGTT TTGCAGGCTA ATTGTGGAAT AGCTTGATTC ATGTATCTCA 1320 CTGATTGATA ATGAAGTGGC ATTAAAAAAA CTAGGACAGA TCCTTTGGAA TAAGAGGAGA 1380 ACTTGGAAAC CAGGCCATGT TGCTTGGCAG GAACAGAGAG GAAGAGGCGA CTTGGCAGGC 1440 AACAGGCTAT AGAGGTCCTA ACAGTGTTTG TTCTTTATGG CTCACTGTCT GGCATACAAA 1500 TCCATTGTGC ATATATGCAC ATCAGAAACA ACCCTAAAGA AAGGTGGAGT TGATGTTGGA 1560 ACTCCAGGTG GCTGTGGACT TAAGATTCCA CAATGTATAT GAACCTAAGA GCATGTCACT 1620 CATATTATCT CAGAATTTAG TAAAAATAAT TCTAAGTGTG TGTCAGACCA TGTGCAACAT 1680 ACTGTGTAAA TTATGTCCTT TACAATAATA TTATAACTTT GGCATTGTAA TCCTCATTTA 1740 ACCAAGAAGG AGGCTGAAAT 1760
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