Tag | Content |
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EnhancerAtlas ID | HS091-38258 |
Organism | Homo sapiens |
Tissue/cell | HepG2 |
Coordinate | chr5:56194900-56197680 |
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) |
CTCF | MA0139.1 | chr5:56196843-56196862 | CCTCCAGAAGAGGGCAGCA | + | 6.07 | FOS | MA0476.1 | chr5:56196420-56196431 | AATGAGTCACA | - | 6.62 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_10966 | chr5:56187953-56195941 | CD20 |
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| Number: 1 | ID | Chromosome | Start | End |
GH05I056900 | chr5 | 56196428 | 56196890 |
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Enhancer Sequence | TGAGCCACCA TTCCCGGCCA AGACTTTTGT CTTCCAAGAT GTGAGATGAA CAAAAGTGGA 60 GATGCTGATT ATAGATGCTA GACAGCTTAC CTCTGAAGAG AAAATTAATG TCTTAACTAC 120 ACACACTAAT GTGAAATGCT TACCACTACA GCTCAAGTAT CATGTTACAA AATATTAATA 180 TGCATATGTA GCATTCAAAT ATGTTGTCGA TGTTAGAGTT AACTTTGTAG GTCTTATTTT 240 GCAATAGATA ACTGTCTGCA CAGTCCGTTA CCAAAAGAAC TCCATCGATG ACTGAAGCCA 300 GTCTCATTAG TTGGTATGCA ACCTGACATC TCTATACCCC ATGCCTCATG GCCCTAGGTT 360 GTAACTTATT ACATCTGTAG AGGTAAAACC AGCCTAAGCT GATGTGGCAA GGGATAAATC 420 CTTCATGCCC CAAAATTCTT TTTCCCACAA TGCTGAGATT CCTGTTAGAG TTTATTTTTG 480 AGATAACTAA GTGATAGCTT CCCTTAAGGT CAATTTACTT AATAAGATTT CTCAACATCT 540 ATGTAGACAT ACTGAGAGGA TGAGGGTTGT AACTAGGGTG AAATGGAGAG AAAGGATAGG 600 AGGAGAAATA AAAAGATGGG GAGATATTGA AAAATCTTTG GCAGAGAGTG GCATGACGAT 660 ATTTGTGCGT TAGAAAGAGC ACCCTTGCAG TACCTTGAAG AAAGAATTAC ATGGGCCAGT 720 ACAAAAGGCA GAGAGAAAGT CAGAAGGCAA TTGCAGTATC CAGAACCTAG GTGAAGGTAG 780 CATCATGGGA ATGAGGAGGA AGAGACAAAT CTGAGCGATA TTAAACAGCA GAATTGAAAG 840 ATTGTAGAAA TGATCTTGGG GGAAGGGTAT GCGGAGGATG GAGAATGACA TCGAGGATGC 900 GTCTGCTATC CAGGCTTGGT CACCTGTGTG AACGCTGGTG CCATTACTGA TACAAGGAAA 960 TCACAGGGGG AGTAGGTTGG AGGACAAGAT GTGCTTTGGC CATGTTAAAA TATTCGAGTT 1020 GCCTGGAGGA TATCCAAGTA GAAGTTTCCA GTAATACTGT ATATGCACAT GAGTACCTCC 1080 AGAGATACTT TGGTTGCAAA TAATAAATGT GCAAGCTATT GACATATAAA TGGTCACTGA 1140 AGCGATTGAT ATATCATTTA GGGTTGTACT CAGCTGCACG TAAAAGTGAC TGGACTACAT 1200 AGCCTACAAA TGAGAGAAGG TAAGCAGGTC AGGGCTGGTG TATTAGGCCT AGGGTGTCAT 1260 CAATGTTGCC ATGCTTTATC TTCCCGCTCC ACTCTTCTCA GCATGAGGCT TTCACCCTCA 1320 GGCTCCAACT CTGATCTCCA ATCTACAATC AGGGAAAGAA AAAGGAGAAT AAAAAGGTAG 1380 TGCCTGTGTC AGGAAGACAG AAACTTTCCT TAAAATGCTT ACGAGATTTT CACTCACATT 1440 TCATTTGACT AGAACTCCCT AGCTATAAGG AAGTCTGAGA AGAATGGACA TCAAGCAGGC 1500 AACTCTACAG CATCTACCAC AATGAGTCAC AAGGGAAACG GGGGAGAATA CTCAGGAGAA 1560 TATGTTCAGT GAGGAAAAAC CAAGACCAGA ACCCCGATGA AGACCAAGAT TTAAGGCATA 1620 GACAAGAAGC AGAATAGATA AAGGAGACAA GAGCTCATCT TCAGAAACTA GAAACGCACA 1680 GGGTCAGGGA AATCAAGAGA GGAGAATGTT TTAAAGAAAG GTCAGTAATT TCAAAAGCCA 1740 CAGACGTCAG GTAAGATAAG AACTTAAGTC TCACAAGGTG AATGGCAAGG ACCATTCCAG 1800 TGAAGCCGAC TAGAAGGAAA CATGATCATA GCTGGGCAAG CATGGTCATG GAGATGATGT 1860 GCATAGCCTA CTTTGTCCAG AAGTCTGTCT AGGAGCAAAA GTGAAGGGAA CAACGTGGAA 1920 GAATTATTTG GGCAATTATG CAACCTCCAG AAGAGGGCAG CAGAGTAAAA CTTTTAATTT 1980 GCACTGCCTG CCAGATATCT GAAAATCAAA GGTTATCTCA CCCCTTCCTC AGGAATAGAG 2040 CAGAAATCTC AGTGTTCCCC CTTAGAATAC TGAAAAAAAC TCAAAACTAT CACTAAGAGT 2100 TGCATTTTTC CATTCTAAAA CCTAGATTCT ATGCTTATCT ATTGCATAAC AGGGTATTCC 2160 TAGTCCCTCT ACCCGCTCCT AACAGTCTAC AACAAAAGGA GAGGCTGTAG CAAGATACTT 2220 GATGCCCTTT CCTGGTCTCT TGTTCTCAGA ACCACTCTAC TCTCAGCTGG CTGGGTCATC 2280 CATCCATTCA TCCATCCATC CATCCATCCA ACCATCCATC CATCCATCCA TCCATCCATC 2340 CATCCATCCA TCCATCCATC TGTCCATCCA TCCATCCATA TCCATCCATG CATCTATCCA 2400 TCCATGCATC CTGCCAACTA CTGTTCCTCT GAGCTTTTCA AACTCTATTT CCAGCTAGTA 2460 CTCTGCTACT AGAACATTCA ATGACTATCT ACTGCTGACT ACCTCAAATG TCCATGTTTT 2520 TTAATGGTCT GACCTTATTC TGCCTAAATC TTTATTTCCT ACTATCCGTA ATACAAAATT 2580 TCTGTTCTAC TCCTTTCGTT ACATTCCTGC TCTCTGAATC CATTGTGTTC CACCCCACCT 2640 CTGCACCTTC CCTCACACCA GTGGTTTTCA AACTTTTTGT TCTCAGAGCA GTCAAGAAGT 2700 GCTGCCACAG AACCTTCCAG TCGATTCCCA AGACTGCCAA AACTAGCTGG TGTACTACAT 2760 ACCTATATGG AGCATGCTGC 2780
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