Tag | Content |
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EnhancerAtlas ID | HS062-16062 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr8:124166570-124167560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr8:124167536-124167547 | GGTGACTCATG | + | 6.62 | JUND | MA0491.1 | chr8:124167536-124167547 | GGTGACTCATG | + | 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 |
GH08I123154 | chr8 | 124166841 | 124167440 |
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Enhancer Sequence | GGACTGAGGA GAGTACTCAA GGAAGGACAG ACTTGGAAGG GAGGCTCCTC CCTCCCCCAG 60 GCTTAGGTCA GACCTGGTCA AAGAAGGTGT GGTTGCAGAC CACTGGATAC TGGGGAGGGT 120 CTCAGAGTTG GCCAGGCCAG GGGTAGTCCA TGTCCCCAGG CAGCAGGAAA CAAATCTGGG 180 CACAGAAAAT CCAAGGCTGG TAAAAATGCA CAGGGAGGCA GGGCATAAGG ACCCCGCTTG 240 TCAGGGTAGT GTGCAGGCTG GCCATATCCA GAGAGCCACA AGAAACCACC CTCAGGCACA 300 GGCAAACAGG CCAGCAGGCA GGTGCTCAGA GTGCATCAGG GTGGTACTGC TGGCATGAGA 360 CCCGGAACAT GCCAGTGTCC ATGCTGGGAA GACTATAGTG ACATGGTCAT TGGGCTAGGA 420 CTGTGAAGTC ATAAGGCAAT TGTGCACACT AGGCACATGG TTGGGGCAGA GCACGACTAG 480 ATGTCCCCCA TGCACACGCA CCACTGGTGG GCCGTGAAGC AAGAGCAAGA GTAAGCCAAA 540 CAGCACATTG GAGCAAGGAA GAGAAGCCTT GTTTCTCCTG CAGTGTCCTT CCAGCACCCT 600 CTATTGACAG CTCAGCATCA TGCGCATTGT AAGGAGAAAT ACCTCAAGAG CCCAGCCCAT 660 CACTGCAGAC CTGAGATGAT TGATAACTGC CACGCTTATA CCATTGAAAG TGGCTCCACA 720 GTTTACTTGG TTGGTTGACA GGAATGTGGA CTCAATGTTG GCCTCTATCT AATGAGACAG 780 ATGCCAGAAT TTCCCTGGCA TGATGTGGAT GCAGGTATCC AAAGGCTCAG GGAGGTAGGA 840 ATGTAGGGGT GGATTGATCA CATCTGGCCT CCTCACTCAC CTCCCAATGC CATGCTCTGG 900 GCCCAAAAGC TACTTCCTTT ATGAAGGCAC TGAACAAGGA GCACCCCCAA ACCTGAAAAA 960 CTCTGTGGTG ACTCATGCAA CAAGACATGA 990
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