Tag | Content |
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EnhancerAtlas ID | HS128-08109 |
Organism | Homo sapiens |
Tissue/cell | MCF-7 |
Coordinate | chr16:2924640-2927480 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr16:2925022-2925041 | CGGCCAGGAGAGGGCGCGC | + | 6.08 | EWSR1-FLI1 | MA0149.1 | chr16:2925879-2925897 | GGAGGGAGGGAGGGAGGG | + | 6.03 | EWSR1-FLI1 | MA0149.1 | chr16:2925862-2925880 | AAAAGAAAGGAAGGAAGG | + | 6.98 | EWSR1-FLI1 | MA0149.1 | chr16:2925894-2925912 | GGGAGGAAGGAAGGGAGA | + | 7.04 | EWSR1-FLI1 | MA0149.1 | chr16:2925874-2925892 | GGAAGGGAGGGAGGGAGG | + | 7.08 | EWSR1-FLI1 | MA0149.1 | chr16:2925886-2925904 | GGGAGGGAGGGAGGAAGG | + | 7.28 | EWSR1-FLI1 | MA0149.1 | chr16:2925866-2925884 | GAAAGGAAGGAAGGGAGG | + | 8.06 | EWSR1-FLI1 | MA0149.1 | chr16:2925870-2925888 | GGAAGGAAGGGAGGGAGG | + | 8.13 | EWSR1-FLI1 | MA0149.1 | chr16:2925890-2925908 | GGGAGGGAGGAAGGAAGG | + | 8.32 | Nr2f6(var.2) | MA0728.1 | chr16:2925313-2925328 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr16:2926980-2926995 | GAGGTCAGGAGTTCA | + | 6.22 | Nr2f6(var.2) | MA0728.1 | chr16:2926655-2926670 | GAGGTCAAGAGTTCA | + | 7.64 | RARA | MA0729.1 | chr16:2926655-2926673 | GAGGTCAAGAGTTCAAGA | + | 6.45 | ZNF263 | MA0528.1 | chr16:2925867-2925888 | AAAGGAAGGAAGGGAGGGAGG | + | 6.38 | ZNF263 | MA0528.1 | chr16:2925895-2925916 | GGAGGAAGGAAGGGAGAGAAA | + | 6.57 | ZNF263 | MA0528.1 | chr16:2925888-2925909 | GAGGGAGGGAGGAAGGAAGGG | + | 6.77 | ZNF263 | MA0528.1 | chr16:2925876-2925897 | AAGGGAGGGAGGGAGGGAGGG | + | 7.05 | ZNF263 | MA0528.1 | chr16:2925892-2925913 | GAGGGAGGAAGGAAGGGAGAG | + | 7.21 | ZNF263 | MA0528.1 | chr16:2925884-2925905 | GAGGGAGGGAGGGAGGAAGGA | + | 7.29 | ZNF263 | MA0528.1 | chr16:2925871-2925892 | GAAGGAAGGGAGGGAGGGAGG | + | 7.38 | ZNF263 | MA0528.1 | chr16:2925880-2925901 | GAGGGAGGGAGGGAGGGAGGA | + | 8.08 | Zfx | MA0146.2 | chr16:2926956-2926970 | GAGGCCGAGGCGGG | - | 6.01 |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 2 | Chromosome | Start | End |
chr16 | 2924788 | 2925331 | chr16 | 2926258 | 2926454 |
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| Number: 1 | ID | Chromosome | Start | End |
GH16I002874 | chr16 | 2924941 | 2925150 |
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Enhancer Sequence | GCCTGGCCAA CATGCTGAAA TCCCATCTCT GCTAAAAATC CAAAAAAATC AGCGGGACGG 60 GATGGTACAC ACCAGTAATC GGGAGGCTAC TCATGAGGCT GAGGCAGGAG AATCGCTTGA 120 ACCCAGGAGG TAGAGGTTGC AGTGAGCCCA GATCACGCCA CTGCATTCCA GCCTGGGCGA 180 CAGGGACTCC ATCTGGAAAA AAAAAAGAAA AAAAAAAAAA AAGAAAAGAA AAGAAAAAAG 240 GGAGAGGGGT GTAAAGACGA AGAAAAGGCT CCTCTCTCGT GCATGCAATC TCTGCACTTT 300 TCCTTGAGCT GCACAGAGCG CTGGGCAGGG CCTCATCCGG GTCAGAGCCG GAACCTGGGG 360 ACATTCTGGC CGATGCTCTT GGCGGCCAGG AGAGGGCGCG CGCGGACTCA GCGGCCGCCC 420 GACTGCCTCA CCAGGACCTA GACCGTGCCG GCCGCCAGGA GGGCGGTTCT GCGCCGCAGC 480 CTCAGTCCCT TCTCAGGATG GGGAGAACTT GCTGATAATG TTTTTTTTTT TTTTTTTTTT 540 TTTTTTAACA CAAAAGACCA TTATCAACAG TATAAACAAA CGCATTTATG ATGATCTGTG 600 TCCCCCAATA TTCATGTATT GAAACTTTTT TTTTTTTTTG AGACGGAGTG TCGTGGAGGC 660 CAGCGGATAA CTGGAGGTCA GGAGTTCAAG ACCAGCCTGG CCAACATGGT GAAACCCCGC 720 GTCTACCAAA ACTACAAAAA TTAGGCCAGG CGCGGTGGCT CACGCCTGTA ATCCCAACAC 780 TTTGGGAGGC CAAGGCGTGT GGATCACGTG AGGTCAGGAG TTCGAGACCA GCCTGCCCAA 840 CATGGTGAAA CCCAGTCTCT ACTAAAAATA CAAAAATTAG CTGGGCATGG TGGCGGGTGC 900 CTGTAATCCC AGCCACTCGG GTGGCTGAGG CAGGACAATC GCTTGAATCC AGGAGGCAGA 960 GGTTGCAGTG AGCCAAGATC GCATCATTGC ACTCCAGCCT GGGCGACAGA GAGAGACTCC 1020 GTCTCAATTA AAAGGGCGAC AGAGCGAGAC TCTGTCTTAA TTTAAAAAAA AAAATTTAGC 1080 CAGGCGCGGT GGTGGGCACC TGTAGCCCCA GCTACTCAGG AGGCTAACGC AGGAGAATCG 1140 CTTGAACCTG GGAGGTGGAG GTTGCAGTGA GCCGAGATTT CACCATTGCA CTCCAGCCTG 1200 GGCAACAAGA GCGAAAATCA AAAAAAGAAA GGAAGGAAGG GAGGGAGGGA GGGAGGGAGG 1260 AAGGAAGGGA GAGAAAGAAA AAAGTCCTTG ATGAAGCAAC ACAATCATTC ATTTTATTAA 1320 TTCTTAGCCA TTGAGTACAC GTCTTTTTAG TATTTTGTTA GTTGAAATGG AAAAGAGGAA 1380 ATACACATAC AGTACCTCTG GGCATACAGT TGTCTCTAGC AGAACAATAT GTGCAACTAT 1440 TTGAATTGTG CTATTAGCTA TTTTTTTGTG GAACACTTTT AATTGATAGA ACCACTGACA 1500 AACTGTGGTT ATTCAGATGT GGGTATTTGG CAGCCATCTT CTCAAAAATG AGAAAAGTGA 1560 GGGCCAGGTG CAGTGGCTCA TGCATGTAAT CCCAGCACTT TGAGAAGATG AGGTGGGTAG 1620 ATCACTTGAG TCTAGGAGTT CGAGACCAGC CTAGCCAATA TGTCGAAACC CCAGCTCTAC 1680 TAAAAATACA AAAATTAGCT GGGTGTGGTG GCACATGCTT GTAATTCCAG CTACACAGAA 1740 GGCTAAGGCA CAAGAATCAC TTGAACCCAG GAGGCGAAGG TTGCAGTGAG CTGAGATCAC 1800 GCCACTGCAC TCCAGCCTGA GTGATGGAGT GAAACTCTGT CTGGAAAAAA AAAAAAAAAA 1860 AAGAGAAAAG TGAGAAGTGA GTCTGTCACT TGAAGGAAAA TAACTGACAG TATTTGTTGC 1920 CAAGGATAAA ATTTAAAATT CTAACTTTTG GCTGGGCACA GTGGCTCACG CCTGTAATCC 1980 CAGCACTTTG GGAGGCCAAG GTGGGTGGGT CACCTGAGGT CAAGAGTTCA AGACCAGCTT 2040 GACCAATATG GTGAAACCCC GTCTCTACTA AAAATACAAA AATTAGCCAA GCGTAGTGGT 2100 GTGCCCCTAT AGTCCCACCT GCTCGGGAGG CTGAGACAGG AGAATTGCTT GAACGCGGGA 2160 AGCAGAGGTT GCAGTGAGCC GAGATCGTGC CGCTGCTCTC CAGCCTGGGC AACAGAGCAA 2220 GACTCCATCT CAAAAAAAAA AATTCTAACT TTCAAGCAAA AATTAAAATG TTGGGGCCAG 2280 ACACGGTGGC TCACGCCTGT AATCCCAGCA CTTTGGGAGG CCGAGGCGGG TAGATCACCT 2340 GAGGTCAGGA GTTCAAGACC AGCCCGGCCA ACATGGCAAA ACCACATCTC TATTAAAAAT 2400 ACAAAAAATT AGCCAGGCAT GGTGGTGGAC ACCTGTAATC CCAGCTACTC AAGAGGCTGA 2460 GGCAGGAGAA TTGCTTGAAC CCGGGAAGCG GAGGTTGCAG TGAGCCGAGA TCACACCATT 2520 GCATTCCAGC CTGGGCAACA GAGTGAGATT CTGTCTCAAA AAAAAAAAAA AAAAGTTAGA 2580 AAACTTGTAT TTGACACCAT TCATTTATAT TATATAATAA AATATGTCAA CATTTCATAA 2640 GATGTGCATT ATTCAATGAA CCAATATTTT CTAAAAAGCC AATGCATGGT GTTATGAGAC 2700 CACACATGGG TACAAGATCC CTCCAAAATG CTAAAAGACC AGTGGATTAT TATTATTATT 2760 TTGAGACAGG GTCTCACTTT GTCACCCAGG CTGGAGTGCA GGGCTCAATC TCGGCTCACT 2820 GCTGCCTCAA GCTCCTGCGC 2840
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