Tag | Content |
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EnhancerAtlas ID | HS158-28765 |
Organism | Homo sapiens |
Tissue/cell | Pancreas |
Coordinate | chr2:2849720-2852490 |
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) |
POU2F2 | MA0507.1 | chr2:2851060-2851073 | TACATTTGCATAT | + | 7.12 | ZNF263 | MA0528.1 | chr2:2852398-2852419 | CTCCCCCCGTCCCCCACCTCC | - | 6.05 | ZNF263 | MA0528.1 | chr2:2851195-2851216 | GAAGGAAGTAGAGAAGGGAGA | + | 6.32 |
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| Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
SE_33649 | chr2:2847186-2856385 | H2171 | SE_66981 | chr2:2847186-2856385 | H2171 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I002846 | chr2 | 2849874 | 2851350 |
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Enhancer Sequence | ACACCCAGAA CTGTCTCCAA AACGGGAAGC GTGTTAGCTG GAAACGACTC GTTCCTAGCA 60 AGGCTGCTCC ATCTGCATGG GCTCGGCGCT GCTGGGATCT GGGATCCGTC CTGACTTGTG 120 ATTCTGGTGC TGTTGCCTTG GGATCCTCGC TGAAATGCCA GCCACTACGT TGGCTCCCTT 180 ATAATCACCT CTTGCCCACT AGGGAAGGTA AAATAGCATC GAATCAGGAG GAGGAGGCAT 240 CGGAAGCACT GTGATGGGGA CGTGGTTAGG TTTTCTTCCT CCAGCCCTGA ACAGGAGCCT 300 CTGAATTTTT CAACAGCTGT CTTTGCCCCT CTTGGAGAAA GCCCCGTCTG TTCCCCCTTC 360 CTCACTGCGT AATCCTTCCC ATACGCCCCT GCTCGCTGCC ATTTCTGAAG GACACAGGGG 420 GCTTCTGTTA CCTGAGCCCT TTTTCCCTCA CAGATGCCTG CAGGCTGAGG CTTGCTGGGG 480 AGGCCTCTTC AAGGGACGCC TAGCCCCTGG ACATCATCCA AGTTGGCAGC TTCACCACAG 540 AGCTGCTGAG AGAAAGGCGC GGGGGGCAGC CTGGGCTGGC CTGCTGAGCC AAGATAAAGC 600 TGCAGGAACC TGCTGCTGCC AGAAGGGATG TTTGCTGGGT TCCCACAGGT GACCAATGCA 660 GGCAGAGACC AGCCAGGACT CCAGCTCAGG GACAGTGATG GGCACAGGGT CACGCAGGGC 720 TCTAGGCTTG GCCCAGGTTT TGAGCCAACA ACACCAGCTG CCTGGTGGTG GGAACAGACA 780 CAAGCACCAG GCTCAGTTTT CAAAGCTCTC CTCCTCCTTC TCCTGTTATT TAAGGTCATA 840 CCACATTGGA AGTGAGTCAG GCAGGTGGAG CCCTTTATGT CCATGAGGCA GGTGCAGCAG 900 CCCAGGGAGG CAGGGTGGCC TTTCCCAGGA ATAGCCAGCG TCACCTGGAG GCAGAGCCAG 960 GCGAGGGCTG TGTGGGTGGC TCCCAGCCAT GTGGACAGCA GGCCTGACTG TCCCTGTCCC 1020 CATGAGCCTC ATGAAGGTGC CGCGGATCCG TCCAGGCGTG GGTGTTGTTC TCTTCCGGCC 1080 CAGCCTTCTC CCTCTTTCCA CACACACGAT TGGGCCAGCA TCTCCCGTCT GCTGCCATCT 1140 CCTCTGCTGG TGGGGGTGCG TCAGCTGACC CTGTGCCCTC TGGCCTCATT TTTCATGGGT 1200 GTTGCCACTG TCTGGCTGTC TGCCCCTTCC CACATTAACT CTCACCCTCT GGCGGCAGAG 1260 ACCTTGTCTT GCCCATCTCT GTATCTCCAG CCCCCAGTGG CCCTCAGTGC GCATTTGCCA 1320 AGGGAAATAT ATGCAAAAAG TACATTTGCA TATCACAGCC CTGTGAGGCA GACACACCCA 1380 GAATCATTGC TCCTGCTTTG CAGAGAGGGT CTGTCCCTGG ACCCCGTCTT TGACTGCTGG 1440 GGCCTGAGGG TGTGGGCGGA CAATGAGGCA CATCAGAAGG AAGTAGAGAA GGGAGAGTGA 1500 GAGCCTGTCT TTCGTCCAGC TCCCTCCCTG CAGGGCCACC CCTGGCCAGC CTTAGACCAA 1560 AGGACACAGA TGCCAGCAAA TGTCTCTGCC AGCCCCCGGG GCTGGCAGGT GGCCTCCCTC 1620 CCAGCCACAC TCAGATGCCA TGGCTGTGAT TACAAAGAAC ACAGGGACCA GGGCACTTGG 1680 GCTCTGTGTG ACAACCCTGT GCAGCTGGGG ACACACACAC ACCACAGCAT GCCACATATA 1740 CATACACACA CACACATCAT ACACACCACA GCACAGCACA CACACAAACC ATACACACCA 1800 CAGCACAGCA CACACACACA CAAACCATAC CCACCAGAGC ACAGCACACA CACAAACCAT 1860 ACACACCACA GCACAGCACA CACACACACA CAAACCATAC ACACCATGGC ACAGAACACA 1920 CACACAAACC ATACACACCA TAGCACGGCA CACACACAAA CACAAACTAT GCACACCACA 1980 GCACAGCACA CACACAAACA CAAACTATAC ACACCACAGC ACACACACAA ACACAAACTA 2040 TGCACACCAC AGCACAGCAC ACACACAAAC ACAAACCATA CATACCACAG CACAGCACAC 2100 AGACACACGC AGACCATACA CGCCATAGCA CAACACACAC ACACAAACCA TACACACCAT 2160 AGCACAGCAC ACACACACAA ACACAAACCA TACACACCAC AGCACAGCAC ACACACAAAC 2220 ACAAACTATA CACACCACAG CACAGCACAC ACACACACAC AAAAACCATA CACACTACAG 2280 CAGAGCACAC CACACGCACA AACACAAACC ATATACACCA CAAAGGAGCA AACCACACGC 2340 ACAAACGATA CACACCACAC CATAGCAAAT CACACACAAA CATACACACA TATACCATAC 2400 ATACCACAGC ACATCACACA CACACACAAA CCATACACAG ACCACAGACA CCACACACTA 2460 CACACACCGT ATCACACATG CCATGAGTGC ATGCCACATG AGTGCACGCC ACAAGCATGT 2520 ACCCCACATG CACACACATA GACACACACA CCACCTTTCC CACCAGCACA GCCGCCCTGT 2580 GGTTGGAGGA GGCTGGGAGT GGTCTTTGCT GTTTTTTGCT TAGGAAGCTG TGAGCCCAGC 2640 ACAAGTCCAT GTGTCTCCTC CCCTGCGGCA CACTTTATCT CCCCCCGTCC CCCACCTCCC 2700 TCTCCCATCC CCTCTCTCTC TCCCCACTGT GGTCCTGGGC TCAGGCTGAC AGGAATCCTA 2760 AGAGGCAGGG 2770
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