Tag | Content |
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EnhancerAtlas ID | HS012-05091 |
Organism | Homo sapiens |
Tissue/cell | Caco-2 |
Coordinate | chr11:86107460-86108660 |
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) |
SREBF2 | MA0596.1 | chr11:86108328-86108338 | ATCACCCCAT | - | 6.02 |
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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: 1 | ID | Chromosome | Start | End |
GH11I086394 | chr11 | 86105847 | 86107750 |
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Enhancer Sequence | TTGCTGTGCC ATTAACCACT GTGCATTTCA GGTGGAGGAA GTTTGGGGAA TAACAACTAG 60 CTTCCTAAAG CATTATTACT TTAGGAAGTA TGAGTAAAGT ATAAAAGTAT GAGAATTTCT 120 GAGATGTTTT GAGTGTGACA TTCTCTTGTT TGTTGCTTTG GAACAACCCC CTCCTGGAAG 180 AGCTGTATGA CACATACCTC AGAAGATTCA GTGTGAAGTC CAGAGTAAGC CTTAGAGGTT 240 GTTTTCCAAC CGCCTCATCT TGCACACGAA ATGGCCATGC AACTAATAAG CAGCCAAGCT 300 TATAGAAATA AAACCATGGC TCCTGGTCCA GTGTTCTTTC CATTGCACCA TATTGCCTTA 360 CTCACTAAAA ATAAATCAGT GGATTGAAAA GAATTTTATT TTGATGGTTT CGGAAGGCAA 420 ACATGGCTGT TCCCTTTGAC ATATTTTGGC TTAGGCACTC CAGGAGGGAA ATAATTATAG 480 TGGGTCAAAG AACAGAGATG GAGTCGCCAT CAAGTCAAGG GCCTAGAAAT GGACATGGGG 540 ACTTAAATAC TCAAAACAAT TGTTGGTGTT TTATTTATGT GACATTTGGC CCCTGAATTG 600 ACTGAAGGTA CCCCCACCCC CACTCCCTAC TCCAACCTAG TACTCCATAC CTGAGGCCAA 660 AGAAATCCTA CAACTACACA CACCAACTGA ACATCCCCCT TCCTCCCTGC TGCAAATTGT 720 AGCTTTGCAA GTCCTTCACT TTTGCCTGGG GAGAGAATGA TGAAGTGAAG TGGCAAAGGA 780 GGGAGGAGAC AAATGGTTAT TTTGGGGCAT ACTCTACCAG GCTATGAATC TTTGCCTTCA 840 AGCTATCCAA CAACCTTTTT TCCACTGTAT CACCCCATAG CATCTAGTTA AAGAAGTAGG 900 ATATAAAAAT TCAAATTGAA ACAAAAACCA ATAACCTAAA TAAAGGACTT TAAGGCAATT 960 TCTCTATATG CAAGCTGCTT TGAGACTATG GTATAGAGGG AAAGGCCTTG GTCAGCTTCC 1020 AGAAAGCCTT GGAGAAAATT AATCTATGAT ATGTACTTAG CACATCAGAG CACTCACCCC 1080 TTGAAGAAAG TGGGCTTATT TCAGAATCAG CCAGCTGGCT GGGTTGCTTC CAAAACTTGA 1140 GAGTTCACAC AGTTACCTGT TCAGGTTCAG TGCAGCAGAA AAACATATTG GCTCATTCCT 1200
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