| Tag | Content |
|---|
EnhancerAtlas ID | HS062-02677 | Organism | Homo sapiens | Tissue/cell | GM18486 | Coordinate | chr11:18000920-18002020 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MEF2C | MA0497.1 | chr11:18001839-18001854 | GAGCCAAAAATAGAT | + | 7.08 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| Enhancer Sequence | AGGTGATCAT TCATAAGAAC ACCTGCAGGG TCTTCCATAA ACCAGGCTCC AAGCCACCAC 60
CACAGCCTGG ATCCTAGACT AGGCAGACCA CCAAATAGTG GGGAAGACAC CTGGGGTAGC 120
ATTGTGTGTT TGTGTGAGCT TCCCCCTGCC AGACAGCAGC TCCTCCGGGC AGGGTTATAT 180
CTTTTCTTCT CTATCTCCAG GCCTCTTAAC ACCTGGCCAG AGGCGCTCAG TGAATGCAAG 240
TATACAAGTA GATCCTTTAG GTTTCTGCAC AACATGGGAC CTGTCTATTC TTTGTGGACT 300
CAACTGATCA TACCCTTGGC TCTGTCTGCA GCCTTCCTTT ACAGTGTAGA CCCTGAAAAA 360
GCACATTGTG TGACTTTAAC TAGGTCGCTT GCTTTTCCAG GCCTCTATCA TCGCACATCT 420
GCAGCATACT AGGGTTTTAC TGGATGATCT TCGAAGTCCT TTTAATTCTA AAATGCTAGA 480
ATTTGAAACC CCCAGGCAAA TCAAGACTGA TCTTCACCTG CAGACACAGC CGCTAAAAAA 540
TGGGAAAGGG GAAAGTAATC AAACAATGCT TCCCTCTAGT GGTTCAGTGC TGTCATTACA 600
CCCTACCTGC GCAGAGACCC TGTCACTCAA CTTCTACTCC AATTCACCCT GAACTCTGAA 660
TGAAAGAAAT CAGCCTGCAG CCAGCAGAGC CCAAGTGCAG GGGAGCGGGA GAGAAAAGAA 720
AGAGGCCAGG CTCAAGAAGC CAAAGAGGCC TCTTAGCCAG TTCCACAATA GTGGAGAAAT 780
TATCCATCTT TAGGAACAAA TATATTTTGC AACTTAAAGG ACCTTTTGTG ACCTCCAACT 840
CCCCTCTTCA GATGAAGAAA CTGAGGCTCA GGGATATTCA GGAGGGACTT ACCCAAAGTC 900
ACAAAGCTGA CTCATGACCG AGCCAAAAAT AGATGGCCAC TCTCCTGCCT CCTGCTAAAG 960
TATCTTGCCT CTCTTCCATG CAACCTCCGA ATTGAGGCCC GTGCAAGTGA CTTGTCAAGG 1020
ACATATATAC ATGGGAATAG ATGGCAAAGG AGCCAGTCTC TTGCACTGAG GGGTAAGTGA 1080
TCTTATTAAC TTTAAAATAG 1100
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