Tag | Content |
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EnhancerAtlas ID | HS184-13752 |
Organism | Homo sapiens |
Tissue/cell | T47D |
Coordinate | chr17:48028650-48030930 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CDX2 | MA0465.1 | chr17:48029297-48029308 | TTTTATGGCTC | - | 6.14 | ELF5 | MA0136.2 | chr17:48029730-48029741 | ACCAGGAAGTA | + | 6.02 | ZNF263 | MA0528.1 | chr17:48030506-48030527 | GGGGGAGTGGGAAGAGGGAGG | + | 6.89 | ZNF263 | MA0528.1 | chr17:48030515-48030536 | GGAAGAGGGAGGGGGAGATGG | + | 6 |
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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 |
GH17I049951 | chr17 | 48029199 | 48030978 |
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Enhancer Sequence | GGTGACCTCA GGTTTCTCAG CACCCTTCTT CCAAAAAGCA GCTTTTTTGG AACCACTTGT 60 CCGAGTGACT TGCCTCAAGC CTTCATGTCA TAGACCCTGC TGCTGTCGCC TCCAGATGCG 120 GCCCCTGCAA GGCCTTATGT ACACCCAGCT CTCAGCGGGG TGCCAGCCTC AAATTCTCCT 180 GTTTCCAGCA CTTGGCACAG AGACCCTCAC AGTTCCCCTT GACCCCCCCT GACCAAGCCC 240 TCCACGCAGG CAGCCAGGCC CAGCTGGAAT AACACGGCTC CGCTCCCTCC TCCCTCCCAC 300 GAGTACTGGA CTATTTACAA CTCACCAGGG CCTTCACACC CATGAGCTCA CTGGAGCCTT 360 CCCCACCCAC CCTGGAAACC CAACAGGGCA AACACCATTA GCTCCATTTT GCAGATGGGG 420 AAACTGAGGC TAGGTGCCCC GCCCAGTGAG TTCCCCAAGG CCCAGCCTCC TAACTTCTTA 480 GTTTGAAGCT CTTCTCAATT CCTCCAGGAG GGTGGCCCAA ACACCCCAAA TTCAAGTCGG 540 GGAGTTTCAG GCAGACGGAA GGGTAGGATC TGATGAGTAG GATCTGTCAC AGGAGCTGGA 600 AGGAGCCTCT CGGGCAGTGA GCCAGGACGG CGGGGGTGGA GGGAAGTTTT TATGGCTCCA 660 GCCACTGGCT GGGTGACAGC CTGGCAGGGG CTTCTTCAGG GTGGACATGG GAGCGGGGGG 720 CAGGAGTGCT GGCCAGCCAG GCAAGCTGGC TGGGAGCACA GTTGGGGTGT CTGGCTCCCC 780 AGAGTAGAGT AGGGGGAAGG GGGCAAAGCC CCAGCCTCAG AGCTGCCTCC TGGGCAACCA 840 GACATGGGAA ACTATAGGCT GGCTGCAGCT GCAGAGACAC TAGGTAGATA CCAAAGGGGA 900 CTTCCATCCA CAGACTCTTT GCTCAGGCAG AGTTCCTGTG CACTGTGAAC CAGGTCCAGC 960 CCAAGCCCTC GCTTGCCATC TCACACAAGG ATTATGCCAC TGTGGACTTC CCACCTCTCC 1020 TCACCTCCTA TATATCTCCC AAGAATTTGT TCCATCCTGG GTCCTCCTAG TCACCCACCC 1080 ACCAGGAAGT ACTCTCCCTC CTAGTCTGCA CCAAAGTCCC CGAAGCCCTG CCAGAAGCCC 1140 TCTCTAATTC TTCCTCAGGT TCTGGACATG ACTCTTTTCC AAGCCTAGGA AAATATAGTT 1200 TGAATCCTCT TGATTCTTTG TGTCAGAGTC TGTGTATGGG GTAGGGGGTT AAAGCTAAGA 1260 GTCTCTCATA AGGCTAAGAG TGCCTGGGGA AGAGGACTGC GTCTCCCCTG TCAAACTGTG 1320 CAAGCCTCCT TCCTCTAGCT GTACCTCCTT CTGCTGGGGC AGGCTCTGCC CATAGGGGGC 1380 GCGCAAACAG TGTTGTTAAG CCCAGGCATC CTTGCTACTT ACTGAACCAC CTGCAGGGAT 1440 ATGGATCTGG GTGACCTGTC AAATGCACCT CCAGAGCTCC AGCCTATGTT TCAATTGGCC 1500 TTGGCTCAGC CTTACTTTTC AACTGGACTG ATGGGAGGGG AGAGGTTTTA GATAAGGACA 1560 GAGGCCCGTC TTTTGGCGTA GGAAGCTGGA GGCTAGACAG TGACCTCTAA AGAAGTCTCC 1620 TTGACCTTCC AAGCTCAGGG TGGGTGAGTG ACTTGAGGTG CTCACACAAC CCACAGTGGA 1680 CCCAGATATC TTCCTTGGCT CTGTTCTGAA TGTTCTGGGC TCCTGGGCAG AGGTCCCAAC 1740 CAAGCAACCC CTATTTCCTT CCCCAAGTCT TTCGGAAAGA CTGGTGAGTC AGCTGCGGCC 1800 ATGAACTCAT CCTAGGCAGT AAAAATAGGA AAACAAACAG GCTTCTCCTC CAGGCAGGGG 1860 GAGTGGGAAG AGGGAGGGGG AGATGGGTTT TTTCCCCTGC TGGGGGAAAA GAGTTGCCAT 1920 CTTTTGAAGT CCTCCAGAGT GAGGCCGGCG TCCTTATGGC CCCTAGAAAC TCAACCACAT 1980 CAAAGTCACC CAAGGAAGGT GGTTTAAGAG GGATGCTGGG TCACACACAC AGTCACAGTC 2040 ACACACAGTG ACACAGCCGA GTCCCTCAGA GGAGCATACA GTGACACACA CAGGAGGGTG 2100 CGACACCCAG CTACGTACAC AACATGCAAA GCCAGTAACC CACCAGGCAG TTGCGTGGAT 2160 ACAGTCACAC AGAAGAGAGC CTAGCCAGAG TCTCCCAGGC CCACCTGGAG ACAATATCAG 2220 AGTCCCATAC AGTCACATCC ATCCACGACA GCTGTCTCCA CGCAGAGCTG CACCTACATC 2280
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