Tag | Content |
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EnhancerAtlas ID | HS095-27805 |
Organism | Homo sapiens |
Tissue/cell | HMEC |
Coordinate | chr7:44263640-44266040 |
SNPs | Number: 1 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOXP1 | MA0481.2 | chr7:44263698-44263710 | AAGTAAACAGAA | + | 7.22 | FOXP2 | MA0593.1 | chr7:44263698-44263709 | AAGTAAACAGA | + | 6.32 | ZNF263 | MA0528.1 | chr7:44263949-44263970 | GATGGAGGGAAAGGAGGGGGG | + | 7.4 | Znf423 | MA0116.1 | chr7:44265179-44265194 | GGCACCCAGGGTGGA | + | 6.7 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 3 | Chromosome | Start | End |
chr7 | 44265119 | 44265222 | chr7 | 44265366 | 44265766 | chr7 | 44265932 | 44266034 |
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Enhancer Sequence | TGCAGTGCTT TTAAACAAAT TGTAATTAAA ATGGGAGTTG ATGGGAAGAG AAAGCGTGAA 60 GTAAACAGAA GAGGAGATGC ATGGTCAGAG TTCCAATCAA GAGTGGTAAC CGTGCTGAAG 120 TACGGGAAGC AGGTCCGTTG TGAGACCCAC CCACCCATTC CACAGATGGG AAGCCTAGGC 180 TGCCCCTGCC CTGCGGAATG GCGCTGCCCA GACCCCAGCT CAACCCAGCC CCCACTCTGC 240 CTCCCCACAT AGCACATGGG AGCTTTTGTG TCCTTGATAT CCAGGCCCCT GAAGAAGGGC 300 ATGATCCCTG ATGGAGGGAA AGGAGGGGGG CCCAACATGA AGAGGTGCCC GGGTCGGGAA 360 ACCTGCTGGC TGAGGACAAG CTGTCCTGGC AGTTCCAGAG ACAAAGGGGA GGTGGTGGGC 420 AGGGCCTGGG CTTGGAGGGG TCTGCACGAG CCAAGAGCCT CTGCAAGTCA GGCCTTCCAG 480 GTGCCCTGAC ATGAACAGGA GCCTTTGCAT TGCCTGTGGC TCTCTTGGGG TGAGGCAACA 540 GGTCCAGGCA GGCCTAATGC GTCCAGGTGG GGTCAGAGCA GGTTCTCATC CTGGCCTGGA 600 CTCCTGGGAC CCCAGGCTGG CCCCAAGCCC ATCTCTCAGA GCCAGAGGTG GCTGCGGGAG 660 GGAGGGCAGC TGCCCAGGGA TCAGGCTGGA TTGTGTATAA TCCGCGATTA GAGAGCGTGG 720 GTGGGGAGGA GACGGGGCCT GAGGCGGGCC GTGGGCACCT GCCCTATTTA CACAGCTGGT 780 GGGTGCCTTC TGGAGAAAGG AGGTGGAAAG GAGGCAGAAA GCTGGCCACC TGCCACCTGG 840 GCCCAGGTGC CCCCAGGGCA GTACCCAGAC TCTTCCTTTC CCTGAGTTCC GGAACATCTC 900 ACCCACCCCT TTCCCAGCCC TGCCCAGCCC CTCCCAGGAG GGCCACACGA ATCTCCATCC 960 TGCCCTGCTC ACAGCTCCTT CCTGCAGCCC CCTCCTCCCC AGCCAAGCTC AGGGAAGACT 1020 CTGGAAGGGC AGGTCTGTGC TGTGGCCCCT GAAGGTGAGC CTGGACACCG AGCCCCGAGC 1080 TGGCCACTCC ACACCCACCC TGGGCCCTGT CCTCAGAGGA CTCACCCCAG ATACTGCACA 1140 GACCTTGAGG GCAGGCTGCA GTCCTGGGCT GGGGTCATGC CAACCTGATG GGGTGACCTT 1200 CCAGGCAGGC TCCTTTGGGC ACACCCCTCC ACTTCTGCAA GGGCAGCAAG CCCCTTAAAA 1260 TCAGATGAGC TGCTGTAGAA GTGGCAGGTG TCGGGGGTTC TGACCACTCC CAGAGGCTCT 1320 GCGGTGCACC CACCCCAGCT GCACGGCGGC CCCTCCCCAT GCCTCCCTCC TTGAGTTCTG 1380 GTCGCCCAGG CACCCCGACC CTATCAGCAT CAAGAACCTG GCCTCTCCCC TCAGCTGCTT 1440 GCCTCTGATC CCCTCAGTCA ACCCCTGCTG GGGGTCCTCA GCCGACCACA GAAGCTCTGG 1500 GGGTGAGTAC CCCTCCAGGG GCTGCCCCCT GCTCTCTCGG GCACCCAGGG TGGATCCAGT 1560 GCCCCTTTGA GCCTGCAGCC TGCATCCCCC TCCTCGAGCC GCTGCTCCTG TGGGTTCACT 1620 CTCCCCACAC CCTTCTGCCC TGGCCGCCTG CAGCAGCCCC CAGGCCCAGC CTGCAGAGGG 1680 GACGGTGGCA AGCAGACCCC ACCTGTCCCT CAAGTACTTA CCTAGCCACT GCCCTGCCAT 1740 GCCGAGCCCG TGGCCCAGCA GCCTCTTCTC TAAGAGTATC TCCACACCAC CCCCAGTCTG 1800 GTGTCTCCCC ACAGGTGGGG GTGGCAGCAG CCCTGGGATG TCATCCATCC CTGTAAGTGA 1860 TACTGCGGGT AGTCGGCAGA CAGACCGGGA GGTGGCCCAG CCTGGCTCCT CCCTGGCCGG 1920 GGAGGCTGCC CAGCCTGTGC TTCCTGTCCC GCCCGCTCTG TTTCAGCCTG GCCCCAGCTG 1980 CCCCCCAGAT CCGCGCCTCC CGATCCCCAC CTGCTCCCTG CTGTCTGGAC TTGGACAGCT 2040 CTAATGCTAG AGCGTCTCAG GCCGGGACTG ACACTTTTCT GTCCCGGCCC AGCAGGTCCA 2100 CCTTGACCCA AGCCAGCAGC TCCTGGCGTG CTAGCCCTTG CCACACGCGC AGACCCTTTG 2160 CCACCCATTC CCCTCCCATC AGGAGAAAGC TGTGGACCTC AGGGTTGCGA ATGCTGGGGT 2220 CGGCAACAAA CCTGCTCTTT CGGACGCTCT TCCTATACAC ATATGTCATA CACACTTCAT 2280 AACCATAACC TCCATTTTCT GAGACCCAGT GGCACCTTCA TGTGCTTCAA AGCAATTCCC 2340 TGGGACCCAG CAGAGGGATC CTGTGCCCCG CCCTCCTCCG CAAGAATGGC CCTTCCCAGA 2400
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