Tag | Content |
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EnhancerAtlas ID | HS127-28429 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr7:27411280-27412810 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
EWSR1-FLI1 | MA0149.1 | chr7:27411901-27411919 | GTGAGGGAGGAAGGAAGA | + | 6.06 | FOS | MA0476.1 | chr7:27412130-27412141 | TGTGACTCATC | + | 6.14 | JUND | MA0491.1 | chr7:27412130-27412141 | TGTGACTCATC | + | 6.14 | SPI1 | MA0080.4 | chr7:27412455-27412469 | CACTTCCTCTTTTA | - | 6.65 |
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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 |
GH07I027372 | chr7 | 27412061 | 27412230 |
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Enhancer Sequence | TTTTGCCCCT CTGTTTAATA ATTGCACTTG GGACATAAAC TCCCCCAGCA GCTCCATAGG 60 TCCTTGTCTT CCAAGGGCAT GGTGTGATCC ATAGCCACCT GCTTGGGGAA TCACCCTTTC 120 CCCATGCTTA ATAGGTTACT CAATAGGTTA CTCTAGAACA GTGGTTTTCT GAGTGTATTC 180 CCCAGACCAG AAGCAAGAGC ATCATCTGGG AGCTAGTTAG AAATGCAAAT TCTGGGGTCT 240 TACCCTAGAC CTATTGAATC AGAAACTCGG GGTGGGCCCA GCCTGTGTGT CACAAGCCCT 300 CCAGGTGATT CTAATGCGCC CTCAAGTTTG AGGGCTATAG TTGCAAACAC TGAAGACAGA 360 TGTTGCTCAT CATGCCCAAC TATACATGCC CTGTTAGTCC TCACTCCAAC CGTGGACTGA 420 GAGGATTGCG ATCTTGTGGT TAGCTTGTGT CTTACTCCAT TTGTGTTGCT ATAAAAGAAT 480 ACTTGAGGCT GGGTACTTTA TTGAGAAATT TTGGCTCAAG TTCTGCAGGC TGTAGGATAA 540 CGGTATCAGC ACCTGCTTCT GGTGAGGGCC TCAGGAATCT TCCACTCATG GCGGAAGGCA 600 AAAGGGAGCA GGCATTACAT GGTGAGGGAG GAAGGAAGAT TGAGGGGCAG GGTCAGAATC 660 TTTTAATAAT CAGTTCTCAG GGGAACTGAG AGAGTGAGAA CTCACTCACT ACCACGAAGA 720 CAGCACCAGG CCATTCATGA AGGATCTGCC CCCATGATCC AAACACCTCC CACTAGGCCC 780 CACCTCCAAC ATTGGGGATC AGATTTCAAC TCGAGGTTTG GAGGGGACAA ACATCTAAAC 840 TATATCAAAC TGTGACTCAT CCAAGGCACA CAGTCTCTGC TCCAAAGCAA GGGTGCAGCT 900 CCACCTCTTG CCTCTGGCAG TTTTGAATGA AATAGCTGAA AGCAGAAAGC AGGACAGAAC 960 AACAGCCAGG GGAGGAAGGC CTGAGGCAGC CACCCATGGG ATAGTTAGGG CCCATTGTAT 1020 GTTTCCTTGG CTGTGGAAGT CATATTTCCC TTAGCATTGT TTAAAGTTGT CCAAGATTGA 1080 TAATGGTGAC AAGCCTGCCT CTGTCCCCAT CAGAACTCCA GAGAGCAGGA GTAGCCGATC 1140 TCAGCCATTG GTGCCACCCA CACGGGAAAT GAGAGCACTT CCTCTTTTAC ACACACACAC 1200 ACACACACAC ACACACACAC ACACACACAC ACATCATTAG CAGTTATGGT TGGGCACTGT 1260 CTCACAAGAT CTCACCTCCT ATAGGGCTTG TCCCTTTGTT CATGAGGAAA GATGGGACCA 1320 GAATGCTGTG GGATGCAAAA TCAATTCATT AGATCACAGG GTGCCTGGAA AGTGGTGTTA 1380 GATTTTTGAC TTTAGAGAGA GGGTCTAGCA GACACTCAAC CACTTACCAG ATGTCCCTGA 1440 GTCTACTGCT CAAAGTCAAG ACAGTCTTTC CTTCCAGGGT AACACTTTTG GTAGTCAATA 1500 AAATGTGCAT GACAGCAGAG GGTGGCACTG 1530
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