Tag | Content |
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EnhancerAtlas ID | HS034-13627 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr18:21002680-21003560 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
Myod1 | MA0499.1 | chr18:21002823-21002836 | AGGGACAGCTGCT | - | 7.52 | TCF3 | MA0522.2 | chr18:21003207-21003217 | AACACCTGCT | + | 6.02 | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | + | 6.31 | TP53 | MA0106.3 | chr18:21003119-21003137 | AACATGCCAGGCCATGTC | - | 6.77 |
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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 |
GH18I023420 | chr18 | 21000838 | 21004105 |
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Enhancer Sequence | TTTTCTGTCA ACAACACATT CGGGGTCATG AAGCTCACCT GAGACACACA GCCCCCAGCA 60 TGCACAGTGC AGGGGCAGCA CAGGTCACAA ACACCCCTCC CCCCCCCAAT GCAGAAAGCA 120 CATCAGAATG CCAAATGAGT GAGAGGGACA GCTGCTTGCT CTAATTGCTT TTTCATTTTA 180 CTTGAGTCAT TCATAAATGT CAAAACCCTG TTTTTCATGA TAAATGACTT GAGACACCAC 240 ACCTCAGAAG TGACTATGAC CACAACCCAC CCATGTGTTG CGACACTACA GTTGAGAACT 300 CTGGCCTAAA GGACAAGTCA CTTGGGTGTG ACACATAAAG TCCTTCGGGA CTTGCACCCG 360 CCCCTCTCCA CGGTCAGCTC CTGTCTGTCT GCTATGTGCA GCCACATTCC AGCCACAGCA 420 GATGGCCCAC AGCCTTGGGA ACATGCCAGG CCATGTCATA CTTCTAGGAG TCTGGTTGTG 480 CCATCCTCTT GCCCCATAAT GTTCTTCCCA TCTCTTTGTC TGTAGTGAAC ACCTGCTCAG 540 CCTATAACAC CCAGTTTGCA CATATCCTGT GTGAAGTTTC ACTGACCCAG CCAAGCAGAA 600 CACACCAAAT GTGGGTCCTG CCTTCAAACA GTTTGGTCCA GTACAGTGAT TCTCAACCAG 660 GCAATCTTCC CCTCCAGGGG GCATTTGGCA GTGTCTAGAG AAATGTTTGG TTGTTACAAC 720 CGGGGGAGAG GAGCGGAAGG TATGCCACTG GAATCTAGCC AGTAGAAGCC AGGGATGCTG 780 CTGAACATCC TACAATGTGC AGGGCAGTCC CCGCTGCAAA GAATTATCCA ACTCAATATG 840 TCAGTGGCTG GAATGTCATT CCAAGGTTGA GAAACCCCGG 880
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