Tag | Content |
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EnhancerAtlas ID | HS101-17224 |
Organism | Homo sapiens |
Tissue/cell | HT29 |
Coordinate | chr16:69065020-69066730 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
MEF2A | MA0052.3 | chr16:69066341-69066353 | TCTATTTTTAGT | - | 6.27 | MEF2B | MA0660.1 | chr16:69066341-69066353 | TCTATTTTTAGT | - | 6.32 | MEF2C | MA0497.1 | chr16:69066340-69066355 | TTCTATTTTTAGTAG | - | 6.57 | PLAG1 | MA0163.1 | chr16:69065505-69065519 | GGGGCCCAAAGGGA | + | 6.17 |
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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 |
GH16I069031 | chr16 | 69065356 | 69066476 |
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Enhancer Sequence | GAGCTGCTGC TTTGGGGCAC CTTCCTGGCA AACCTCTTGT CCAGTGATCC TGCCCCACTT 60 CTAGAGACCT GGACTGTTTC TACAGAATCA ATCCCAGGAA TGTTCATGGT CATTAGCAAA 120 TTGTGAGCAC AACAAGGGCA GAACCCATCT TGATTCATCT TGTCATACCC CCAATACCTA 180 TCACAGTGCT TGGCACATAG TGGATGCTAG GTGTTGGCTG ATTAATACAA TATTGAATGA 240 AGAGCAGAGA AGGATGGTTG GGAAGGCTAG TTCCTATGTG TTTCAATAAT AGTCATAGCA 300 AGGCTGGGCA CGGTGGCTCA GACCTGTAAT CTCAACACTT TGGGAGGCTG AGGTGAACAG 360 ATCACTTGAG GAAAGGAGTT CAAGACCAGC CTGGGCAACA TGGTTAAATC CCATCTCTAC 420 CAAAAAGTAC AAAAATTAGC CAGGTGTGGT GGCACACGCT ACTCGGGATA AATTTAGTAA 480 GATAAGGGGC CCAAAGGGAG TTTGCTGTTG TCTCAGATGG ACGGGAAAAG CTTTCCTGAC 540 TAGTGACTTT TTTTTTTTGA TACAGAGTTT TGCTCTGTCG CCCAGGCTGG AGTGCAGTGG 600 TGCGATCTCA GCTCACTGCA ACCTCCACCT CCCGGGTTCA AGCAATTCTC TTGCCTCAGC 660 CTCCCAAGTA GCTGGGACTA CAGGTGTGTG CCACCACACC CAGCTAATTT TTTTTGTATT 720 GTTTTAGTAG AGATGGGGTT TCACCATGTT GCCTAGGCTG GTCTCAAACT CCTGAGTTCA 780 TGCAACCTGC CCGCCTCAGC CTGCCAAAGT GCTGGGATTA CAGGAATGAG TCACTCCGCC 840 CAGCTGACAA GTGACCTTTG AGCAAAGATA TAAGGAAGCA AGGGGTTGAT CCAGAAACCT 900 AGGGAGGGAG CATTCCAGGT GGAGGGAGAT GTGAGTGCAG AGGCCCTGCG ACAGGTGCAG 960 GCTTCACGTG CTGGAGAACA GTAAGGCCAG TGTGGCTTCA GAGAAGAACA GGAGTTGGCA 1020 CCAGAAAGGC AGTGGCCAGT CCCAGTGGAG CCTTGTGTGG ACTTTGGCTT TCCCTGTGAA 1080 TGAGATGGGA AGCCAGGGCG GAAGAATGAA ATGATCTAAC TTCATTCGTT CATTCATTCA 1140 TTCATTTATT CATTCATTCA TTTATGGAGA CAGAGCCTCG CGCTGTCGCC CAGGCTGTAG 1200 TACAGTGGCA CAATCTCAAC TCACTGCAAC CTCTGCTTCC TGGGTTCAAG CAATTCTCTT 1260 GCCTCAGCCT CTCAAGTAGC TGGGACTACA GGCATGTGCC ACCATGCCCA GCTAATTTTT 1320 TTCTATTTTT AGTAGAGGCA GGATTTCACC ATGTTGCTCA GGCTGGTCTC AAACTCCTGA 1380 GTTCAGGCAA CCCACCCGCC TCAGCCTCCC AAAGTGCTAG GATTACAGGT ATGAGCCACA 1440 ATGTCCAGCC GATCTAACTT CTTTTAAAAA GTTACTGTTG GCCGGGCATG GTGGCTCACA 1500 CCTGTAATCC CAGCCCTTTG GGAGGCCAAG GTGGGTGGAT CACGAAGTCA GGAGTTCAAG 1560 ACCAGCCTAG CCAAGATGGT GAAACCCCGT CTCTACTAAA AATACAAAAA ATTAGTTGGG 1620 CATGGTGGCA GGCGCCTGTA ATCCCCACTA CTGGGGAGGC TGAGGCAGAG AACTGCTTGA 1680 ACCCGGAGGC TGAGGTTGCA GTGGGCCAAG 1710
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