Tag | Content |
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EnhancerAtlas ID | HS062-14375 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr6:119121190-119122500 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr6:119121847-119121866 | TCCTGCCCCCTAGTGGTGG | - | 6.73 | ESR2 | MA0258.2 | chr6:119121878-119121893 | AGGACAGGCTGACCT | - | 7.24 | Hnf4a | MA0114.3 | chr6:119121538-119121554 | AATGGACCTTGACCTC | - | 6.37 | Stat6 | MA0520.1 | chr6:119121740-119121755 | ATTTCTGAAGAAATG | - | 6.67 |
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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 |
GH06I118800 | chr6 | 119121192 | 119122485 |
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Enhancer Sequence | CTGGATAAAT GCTTGTTGTT GATGCTGCAA TCCGACAAAG GAGATATTGT GCTGCTTTGC 60 TGGTGTACAG CAGCTTAGGT TTTGGCGGTC ACAAAACTAG TGAGTAGCAG CAGCCAGGCA 120 CCCAATCCAG TGCTCTCTCC ATCCTCACAC CTGTATGGAT GCTAAACTGT GCATCGCTCT 180 GTGCAGTCTA TCACTTGTGT GGGATTCTGG GATTTTTTTT AAAAAAAGCT TCTGATGAAC 240 AATATCCCTT TGAGGACCTG TGGATTTGGA ATCTGAGTGC CTGCTCCCCA CCTCCCAAAA 300 GAATCACATT ATTAAATGTA TATTCTTTCA GATTACAGGT TTCTATAAAA TGGACCTTGA 360 CCTCATGGCT CAGGGGGTTT CAAAGCCCTG TCGCAGCCTT GCTCTCTAGG TATGCATTTT 420 CAAAGTCTTC AGAAGATAGA GCGGTTTTTC CAAAATGATC AAAGGACACG CCTCCTGAGG 480 CGCCCTCCCC TTCTCCTGGC CCACTCCTCA GCTGGCCTCT GCGTCTGCCA GAAGTGCTCA 540 AATGAGGCTG ATTTCTGAAG AAATGTTTTC ATCATAAGAA TTGCAAGCAG GCAAGCCTCC 600 GGCTTTTGCT TGTCAATGCA CGCGTTTCCA GCCTTTTTAG TTCCTTTATC AGATACTTCC 660 TGCCCCCTAG TGGTGGGAAG CAGCAAAAAG GACAGGCTGA CCTAGATACT GTTTCCAGAG 720 CTGACTATTC AGCCGTTAGA GCAATCATTG TTCGAAGCAA GCAAGAGCAG GAAATAAACA 780 AAAACCCTTT CACGGTGGTG CTCCAGGGTC TAGTTGTTAA TTTTTGAGCG AGGAAAAGTT 840 GTTCATGAAA AAATATATAG TATTTGAGCA CATTTGATGG AAAATAAAAA GGAATCTTTT 900 GCAGGGCCAC ACCTCGCCAT CCTCCAGGGT TGTCATTCTC AATGTGCTCT ACGTGGACGG 960 CTCTGCCCTG CGTCGCCAGG TGCTGCCACC CTGCAATGTC ACTGTATTTC TTAGATGCTG 1020 AACCAAGCCC AAGGCAAGGA CTCCCCTGCT CTGGAATGTG TGAGCAGCTG CTGAGGTCTG 1080 CATGTAGAGG AATAATTACC ACTTTCTGTG GAACGAATAC TCAACTTAGG ACCAAATAAT 1140 AGCAATCTAG GAAATTTAGA AATAGTAAAG ATTTTTGGTT TATATGTAAT GGATGTTGCT 1200 GCTGTTCCAA CCTTACAAAG TAAAGCTGTC TGCTTCCCAA ATTCCAAAAA TTAAAATACT 1260 CCTCCACCTC ATCCTACCAA CCAGTGCCCT TTGGCTCACT CTCATCTCGA 1310
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