Tag | Content |
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EnhancerAtlas ID | HS042-13966 |
Organism | Homo sapiens |
Tissue/cell | Fetal_brain |
Coordinate | chr14:68216020-68216940 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myog | MA0500.1 | chr14:68216679-68216690 | GACAGCTGCTG | + | 6.14 | STAT1 | MA0137.3 | chr14:68216743-68216754 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr14:68216743-68216754 | TTTCCCAGAAA | - | 6.32 | Tcf12 | MA0521.1 | chr14:68216679-68216690 | GACAGCTGCTG | + | 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 |
GH14I067748 | chr14 | 68215635 | 68217753 |
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Enhancer Sequence | AAAGTCGAAT TAACGTCTAA CCCCACTTAG ACCTGATTTG ACTCTGCCTG CTTGGACCAA 60 AGGCAGCTGT TGCAGGATAT GCGTATGTGT CTATGTCCCA GGATCGCTAT CTCATGAATC 120 CCCAGCTTGG TGGAGACAAA AGTCCCTTCC TTTCTGGCCC TGGTCTCCCC AGCACCCCCT 180 GGTTAAACAG TGCTCTAGGC TGGTGAGCAG AGAGGCCTTC ATAAGCTGCC ACAGAGCTTC 240 TGCCAGCAGC TCCCTTTCTG CTGCAATAAT CCCTGTTGGT TAGTGGAGGG GACTCGCCTT 300 GCTTCCTGTA TCAATGCTCC ATCTGTTATT TGTTTTGGTC ACTAAAGTTT TTCTTTCCTT 360 TCTAAGCTGA ATTATAGATA ATCTCCTACA GCTAGATGAT GTCTGGCATG TTCTGAGGTC 420 ACTAAAGTGA TCCAGTCCTG TGCCGCTTGG GAATCCACTT GCTGCCCTAG GATGTTAGCT 480 CTCCCCAGGC CTTCAGCTCC CCTTAGCATC TATGTACACT AAGCTAAATA CATATCACAA 540 GTTGGCAGGC AAAATTCCTA CCAAGAGAAG AAGGGCATTT TGCCAGAGAG TCTGGAATGG 600 AGTTGAATGA AGTTGTTTTT TGGCAAGCCC CCATGGCCTA AGCTCATTTA ACTGCATTAG 660 ACAGCTGCTG AGAGAAAAAT ACCTGAAAAA GTAATAAGGA CTGTCTCTAT TTTAGAGCGT 720 GTCTTTCCCA GAAATAGCGT CTCTGTCCTG CTGAGTGGGA GGCTCAGTGA AGGCTTGAGA 780 AAGAACTGCA GTCTGGGAAT CAGAGGACCT GGGCGTCTGT CCTGGCTGTT AGGTTCTCAG 840 TCTGACTCTA GAAAAGTAAT TCTCTACATT TCAGGATGTC AGAATTTCAT CCTTTCTGAC 900 ATCATCATGA TGTTACAGAA 920
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