Tag | Content |
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EnhancerAtlas ID | HS101-06969 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr11:13125770-13127960 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
PPARG | MA0066.1 | chr11:13126360-13126380 | GTAGGGCAAGGGGCCCCATT | + | 6.35 | ZNF263 | MA0528.1 | chr11:13126815-13126836 | TCCCCCACTTCCTCTTCCTCC | - | 7.79 |
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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 |
GH11I013104 | chr11 | 13126074 | 13127458 |
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Enhancer Sequence | AAAGAAAGTA AGAGATGTTT GGATGGAAGC CATGTGAACA AAGGAATAGA GGAAGGAAAA 60 TACAGGGCAG GTTCGGGGAA TGTTCTGCTG TGACTGGAGC AAAGGGTGAA TGGAAATCCA 120 GTATAGGAAG CTGAGGCTGG ATAACCAAAT TACAGCCAAC TGGTGGGAGA GTCTTAGACC 180 TTGAGATTTG GGAGGATCCC TAACCCACCT TCTTCATTAG AGCAATAGAA GAGAAACAAG 240 ACCAGTGTCT TGGAGAGTAT CAATGGCTGG TCAATACCAA AAGGCAAGTA AACGGCAGAG 300 ATGGAGGCTA AAGCTCCTGA CTCTGAACTC CCTCCCCAGT TTCTTCTTCG CTGCAGCGTG 360 CTGCCTCCTT TGAGATGGAT ATGGGAGGCA GGTGGAGTTG GTGATGGGAC AGAGCTCTCC 420 TGTGTGTTGC CCAGCCTCAT TGCCTGCTTT CCTTCTCCAG ACACAGTGTA ATATCAGTGT 480 TGGCTCCAAA CAGCCAGGAG TGGCCAACAT GACACGTACC CCTCTGTCCC TATCCTGTGC 540 TGTCAAGCAC CTTGTATATA GGCTGTTCCC AAGAGCAGAC CAGGAGTGAA GTAGGGCAAG 600 GGGCCCCATT CTTCTCAGCC CAACCAGCAC TGGCCATTTC CTCTCTTGGC ATGATTTTAG 660 AATTTCCCAT TCTCCTCCCT ACTGCATTTC CTGCTCAAAG TAGATTTTTT TCCTAGGTCA 720 ACTCAGCTGC TCTCTAATTC GGGCAAAACT AGAGATGCAG AGAAAAATGA GAACCTGTTG 780 GGGTTATTTT GGCCTATTGT TCCACACTAC AGAGACATTA GATAACGACC TGATCCTGTA 840 CCTCTCCTAC TCCGCCCCAT CCCACGACCC TGGAAGGCAT TGTTTGAGTG TTTTGTTTGC 900 ATTGTTCAGA GGTTCTCTTA ATCTAGTTCA AATTTAAACC TTGATGAAAA AGACAGGTGC 960 AGGCAGCTCT GTGGCTCTCA GTTATTGACC ACTCTGTGCA AAAGCCCACA CCATGCACAC 1020 ACGTCTTTGC ACTGTCCACC ATTTGTCCCC CACTTCCTCT TCCTCCCTGT CTGTCTTCCC 1080 CACTATTAAT CCTTTGCTCC TATCCAGCTG GTCTCTGGAT TATTCCCTGA ACTTGCCTTG 1140 TGTTTTTCCA CCTAAAAGCC TTTGTCCCCA CCACCTGTCC CCATAAAATG TCCTCCCCAC 1200 TTTTTTCCAT CCAGCCAGAT CAGATTCGTT TCACCCTCAT TCAACGCCAA CTGTTAGTTG 1260 GCACTGGGCC AGCACACGTT ATCTCATCCT GCAAGGCCTA GCATACATTT ATTCTTATCT 1320 GGGAAGCTTT CTGGGGCTAC CCCAACTGGA AGTGACTACT TCCTCCTTTC TCTCACACTT 1380 ATTGTCTGTA CTGCTCATTT GGTGCTTAAT ACATCCTAGT ACTTTACAAT TAATCATTCA 1440 CTTGCTCATT CATTCATTTA ACAAGTATTT ACTGAGTGAT TATTATTTTG CAGACACTGT 1500 GGTAGATGCT GGAGAGATGC AGATGCAAAA GACACCCTGG TTGTCCCCTA GAAACTCACT 1560 CTAGTGGTCA AAATTGACAC ATCAGAAGCT GCTTGTCATA AAATGATGAG TATAGGTCAC 1620 ACTTCAGAAG TCCAGCAGTG GGGCTCCATG ATGAATGAGT AAACAGTGGC TCTGTGAAGG 1680 TGGAGAGAAA GCGCATTTTC GGAAGGTAGA GGAAGAGCAG GTGCCCAGAG CTGAGGAGCA 1740 TTGGAATAGG GCTACAAGCA GCACTTGCTG CTGGACCAGA GAATGTTGCC AAAGTATAGA 1800 ATGTGCAAGA TATCATTGGA GGACCTGGAG TTCCAGTCTT AGAGCTTGGC TTCATTCTGA 1860 GAGGCATGTT GTGCCATTGA GGGTTTTAAG CAAGGGATTG ATTCAAGCTT TGTGGTTTAA 1920 GATCACTCTG GCTACTTTCT GAAGGGTGGA TAAAACCAGG GAGAGATTTG AGGCAGGAAA 1980 TTGTTAGGAG GCTGTGGCAA TAACCCAAGG CAAGAGACAT GAAGGTGGTA ATCTCTGCCT 2040 GAGAAATGAA GAGACTCGAT TTGAGAAATA CACAGGATGT ATAAAATTAT ACCGCAGTCA 2100 CAGCTCTGGA GGCCCTCACA ACCGAAAAGT GTGCATAAGT ACAATTCAAT GTATGGAACC 2160 TGTCAAGGAT TAAAAAAGTG CTACCAGAGC 2190
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