Tag | Content |
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EnhancerAtlas ID | HS129-31329 |
Organism | Homo sapiens |
Tissue/cell | MCF10A |
Coordinate | chr6:29781330-29782450 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.32 | JUND | MA0491.1 | chr6:29781808-29781819 | GATGAGTCACC | - | 6.62 | NEUROD2 | MA0668.1 | chr6:29782279-29782289 | GCCATATGGT | + | 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 |
GH06I029813 | chr6 | 29781741 | 29781890 |
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Enhancer Sequence | CCCTCATCCT GAGGCTGCCT CTACGCACCC TCTGCACCTG GGGATTGCCA CTGCCACAGG 60 CACTGTCTCC CACATGGACC CTCTGAGAAA CGAAGCCCCA AATTTGACTT CCTGTTCTAT 120 TCAACATCCT TTACAACATC AGTATTGGGG GAAATCCTAT TAAGATTATC CAGCTGAAAT 180 TATGTTGATG GACACCAATA CTTAAAGCAG GAATTTTGAG AAACTAACAT GTAATTTTCA 240 TGCCTTTTTC TGGCCAATGT CCCAGTGACC TACGAGAAAA CCTTTCCTGC CTACAGGGAA 300 CCAGAACTGA CAATCCCTCT ATAGGAGACA CCGCAGGTGA GAGCAGGAGC AACCACAGAC 360 CTGCACTGCC CGTGCTGTGG TTGCCTCCTG GACGGGGCCC TCTTGCTGCA GGGCAGGGGA 420 TGAACCGTCC CATCTGCCCA GGCCTGAGTG GCCAACTAAC TGTGCAATTA GGTTCAAGGA 480 TGAGTCACCA CCACCTCACT GGCCAGACAC ACGGAAGTGG AGAAATGGCA GAAAGACTCG 540 GGTTTCCTGG ACACCCCAGA CTCTCACTGT CCCCTGCACT GCCTCTGTCT TTGCAGAAAC 600 TCAAAACTTT CTGCTTGCTC TTTTCCTCTC CCCTCAAACA ACCTGACTGT GGGGGAAATG 660 ATTCTGACTG TCTCTTATTG TAAACTTACC AGGCAGCGAC TACACTAAGA ACAAAAACAT 720 TGGCTCAGGA AAGGCAAGGT GAGGCCACAG AGCACAGAAC AAAGCCCAAA AAACAGCCCA 780 CTGGGTACTA TGACCCTCGG GGGCTGGAAA AAGTAACACC TGGACATGGG ATGAAAACAG 840 GGACCACAGC TGCCCTGACA GAGGGCTGGT CCCCACTCCC CAAATAGCCC AGGGACATCT 900 GCTTATCAAC TGGTCCATAT TATCTGCAAG GAAACACAGG GAGACAGGGG CCATATGGTG 960 GGAACCCAGA AAAAGCACGG TCTCGAGGGA CCCAGAGGAC GTGACACCCC TGAGACAGCT 1020 CCCAGATGAG GCATATGGGG AGCTGCAAAG TGGACAGAGG ATGGCCATGT GCACTCAGGA 1080 CTCTCCCTGT TACAAGGGGA CCTCAAAGGG GCTGTACACA 1120
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