Tag | Content |
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EnhancerAtlas ID | HS018-13292 |
Organism | Homo sapiens |
Tissue/cell | CD19+ |
Coordinate | chr2:178145460-178148100 |
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) |
EWSR1-FLI1 | MA0149.1 | chr2:178145601-178145619 | TATTCCTTCCTTGCCTCC | - | 6.22 | Foxd3 | MA0041.1 | chr2:178147938-178147950 | GAATGTTTGTTT | + | 7.22 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_26714 | chr2:178146124-178148074 | Esophagus |
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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 |
GH02I177281 | chr2 | 178145928 | 178147728 |
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Enhancer Sequence | AGTTTAGATT CTCGTAGATG TGTGTAGAGG TAGGGCTGGA AGTGGAGGTG GGTTTGGGGG 60 TATGTTAAAG CAATGTATGC AGGAAAGAGA ATATTAAAGA GAACTTACAC TGACAATTTT 120 GCCTGGCTGG GATTCTTGTG TTATTCCTTC CTTGCCTCCT GATTTCCTTC CTTTTTTTTT 180 TTTTTTTTTT TTTTTTTGAG ATGGAGTCTC TCACTGTGTC ACCCAGGCTG GGGTGTGGTG 240 GCATGATCTC AGCTCACTGC AACCTCCGAC TCCCTGGTTC AAGCTATTCT CCTGCCTCAG 300 CCTCCCGAGT AGCTGGGATT ACAGGCATGT GCCACCACGC CCAGCTAATT TTTGTATTTT 360 TAGTAGAGAC AGGGTTTCAC CATGTTGGCC AGGATGGTCT TGATCTCCTG ACCTCATGAT 420 CTGCCCGCCT CAGCCTCCCA AAGTGCTGGG ATTACAGGCG TGAGCCACCA TGCCCGGCAT 480 CCTTCCCTTC TTTAGTTTAC ACACATAGGC CCCAGGTACA GGGCATGAGC TAGAGCTGGA 540 TCCCAGCTGA ATGGAAAGCA GGAGGCGCTA TATTGGAAAC AACTGCCAAG CAACCAAGGA 600 CTGGGGACAA AATAGCCTGG GAGGAGAAGT AAAACCAGGA AAAAGTTTAA AATTAGGTGC 660 CTGACATTTA AGGGAAAAAG TCCAAAGTTA ATCAAGGATG ACCGCTTATT GCAAGATTCA 720 AAACCTCTAA ATGACAAAAC TTCTAAAAAA GGAAATGATG ATAGCACGGG GAACCCTGCT 780 GATCCATCTC CCTGCCCAAA TACTTCTCCA TTCCCAACAT CTGTGCAGCC ATGTGCAGCA 840 GAGACAAACA GCAGCAGCAC TCCACCCCCA AGCTTTGAGA ACCGCAGAGC TGTGGCTGAC 900 ACAGTGGTCC TATCTCTGTG AAGTACACAA ACCATACCAC AGCCTTATTT TCTGAGACCA 960 TCTCTATGTA ACCAGCTTCC CTAAATGCTG TGGCCCAAGA GGCTAACACT TTGGTCAGTC 1020 ATGGGGCAAT ATGGCTGCTC CCACATGGCA TCCAAGTCCA TGCTTAGAGA CTGAAGGGGA 1080 GCCAGCCTTG GTAAACCAGG TCTGTGGTCA TTTCCCCACC TGGCATTTTT GAGCTGTACC 1140 AAGCAGCCTA GGGGTTCTTA CTGCAAGGGC ACGCTCAAAC CTGACTTGTC CAGACAAGCA 1200 GAAGAGTTTT GGGCTCCCAA TCGAGCACGG TGGTCAGTCT GTTCCAGTTT GTCTGGGACT 1260 TTCCAGGTTT GAACACTGAA AGTTCTACAG CCAGGAAATC CCTCAGTCCC AGGCAAACTG 1320 GGATGGTTGG TCACCCTGAA GTCAAGACAC CTAGGCTTTG GCACCTAAAC ATCAGTTTCC 1380 TCATCTGTAA AATGCTGGGA CTGGCCAGTA CAGCTTCTGA TGTTACTGCC ACATCTAATA 1440 GTCCATGATT CACTCTCATG CTCCTGACCT TACCCATCTG CAGCCCAACT CCCAAACAAA 1500 CTTCACTTGA TCCAAGATCG AGTTCATGTA ACCTGATAAG CTAATCATTA GTGTGTTAAC 1560 AGGAGAGGAT TATAGGGTTC ACAGTTGAAT TTTAACAATG GCTCGGGTGG AAGGCATGTG 1620 GGTAGCTGAG TCGTTCTAAT GGTGGGAAGT TCAGCTGGGG AGATGGAGTG TATGGCTCTG 1680 TGCCATCTGA GAGAAAGATA TTTTTAGGCA GGCAGGTTTT GAGGCAGCCA GCCTGAGAGA 1740 GCTGGTTTGA TGGGCTGCTT TTAGCTGCAC AGCAGGAACA GGCCACAGGC AGGGCAGTCT 1800 TGTCTGACTT GAGCCAACTT TCACACTATG ACCTGAATAA AATCAGCAGT TGAAGCCACA 1860 GACTGGAGAA GAAAGGATGT AGTCTGCTGA TAGCAATATA TATGTATATA ATGCATTTGC 1920 TTTGAGCCTG GGTCTGTCAT CTATAATACA GATATGTAGC TATGATCCTG GGTAGTTGAG 1980 AGTTCAGACT CTGGGATCAC CACCTACCAA CTCTGTGATA TTGGGCAAGT TGTAGACTGA 2040 ATAATATGCA TTTGCTGATA TTTAACCTTT TTGATCTACA CACACAGGAA TTCCACGTGG 2100 TTTAGCCTAA TAGCTTACTC TCTTTTTCCT TGGTTTCCTC ATGTGTGAAA CGCAGATAGC 2160 CACCAAACTT TTCAGGACAC TGTGAGGACC AAATGAGAGG GACACATAAG GTGGTCAGAA 2220 CAGTCCTAGC CCCACAGTCC ATGTCAGTGA TGTCAGCCAC CACCATCCTA CTGGTGAAGA 2280 GGCAGGCATA CAGGGCCATT AGACTCCATC AGCTGAACCT AGGGTAGCCC AGACTCTTCC 2340 TGTCTTCCTG AGACATGGAA CATGGATGAA CCAAAGTGAA TTGGTCACCT TAGCTGAACT 2400 GTAGAACTTC ATTCTAATCC CAGGGTGAGG AAAGGGGAGT AGGTTCATAC CACAGGTTTT 2460 TCAGGTCATT CCAAGACTGA ATGTTTGTTT TTCCTCCCAA TACAATCAGG TCCTAAGTAT 2520 AAAAAAGAGC TTTTTATCAT GAGGTTTTGC TCTAACACCA TGGAGCCCTT TCTTTAGCCT 2580 TACATCTGTC TGTAGCGCCC ACACATGGCC GTCTTCTTCA ACTTAACTAT ATACACACAC 2640
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