Tag | Content |
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EnhancerAtlas ID | HS108-23344 |
Organism | Homo sapiens |
Tissue/cell | K562 |
Coordinate | chr2:134975980-134977270 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOSL1 | MA0477.1 | chr2:134977018-134977029 | GGTGACTCATC | + | 6.32 | JUND | MA0491.1 | chr2:134977018-134977029 | GGTGACTCATC | + | 6.62 | PLAG1 | MA0163.1 | chr2:134976822-134976836 | GGGGCCCAAGGTGG | + | 6.39 |
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| Number of super-enhancer constituents: 9 | ID | Coordinate | Tissue/cell |
SE_10191 | chr2:134974361-134978757 | CD19_Primary | SE_10845 | chr2:134969874-134979987 | CD20 | SE_18527 | chr2:134972393-134978121 | CD4p_CD25-_Il17-_PMAstim_Th | SE_19349 | chr2:134973348-134978300 | CD4p_CD25-_Il17p_PMAstim_Th17 | SE_32531 | chr2:134974671-134976629 | GM12878 | SE_40997 | chr2:134975776-134978786 | Left_Ventricle | SE_58311 | chr2:134974519-135073637 | Ly1 | SE_59645 | chr2:134963734-135083692 | Ly4 | SE_62223 | chr2:134937777-135083863 | Tonsil |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I134216 | chr2 | 134973902 | 134978618 |
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Enhancer Sequence | CTGTGGGTGA GTTGGGTCGT TCTTTTAGTC TTAGCTGGGT TCACTACTGA TGCAGGGGGC 60 AGGGTGAGGG GTCAGGCTGC TGGTCTCAGC TGGGCTTTCT TATGTATTTG AGGGGTAGGC 120 TGGCTGGATC TGGTCTAGGA TGGGTTCCAC GGGGCTCCCT TCCACATGGT CTGCCGTCCT 180 GTGGCAGGCT AGCCCAGGCC ATCTGCTTGG TTCTAAGAAG GAAGTAGAAG CATGCAGTAC 240 CTTTGGAGGC CCAGGTTGGG ACCTGGTGTA CTGTGACTTC TGCATTTTAT CAGCCAAAGC 300 AAGGTGCAAG ACTAGCCCAG ATTCAAAGGG TAAGGATATA GACTTGTTGA TGGGAGTTGC 360 TGTTGAGTCT TATTGCAAGG GGAATGGGAT ACAGGGAGAC TCTTAATTGG GACTATTCAT 420 TCGATTAGCC TGCCACATCC TTTCTTTTAT TCATTGATTC TGTTATACTT CACGTGGTTC 480 CTTAAGCAAT GCTTCATTCT GTTGTTCCAT TCTTTACTAA TTAAAACTTC TTAAAGGCTG 540 TGTATCATTT ACTGTCCATA GTCTCTGGGA AAGCCACAGA GATGAGTAAG ATCCCAGTCC 600 TACTTTGCAG AAGTTGATAA GCAAAGGGCC AGGGGAGATG GACATGTCAG TGGCCAGTAA 660 TTAGAGAATT TGAGGAAGCC CAGGGAGGTG TGAGTGCGGT GGAGTGGGCT GGGAACCCAG 720 AGGAAGTAGC AGCGAGCCAC CTGTCGGGGT GCAGCGGCTT CATCAAGGAG GAGCTCAGTC 780 ACCCAGGAGC AGGAAATGGC TGAGCGAGAA AGCAAGAAGA GAGCACATGT GGCAGGTGCA 840 GAGGGGCCCA AGGTGGGCAA CAAGGCTTGT GTAGCTGCTT CTGCAGTGCA CAGTTTACTG 900 TAGGGGTGGG AGTGGCAGGA GACAAGGCTG GAAAAGCCCA CCTGGGCCAG GTGGGAAAAC 960 CTGCTGTGAG AGCTAAGGGG CTCAGATGTT TTTGATGGCT AAGAAGGAAG TTAACAGGAT 1020 TCTTCTCTCT CCCATGCCGG TGACTCATCT ACTTTAACGA ACAGACAGTT CAATTATTGC 1080 ACCCTAATGC TTTTTCCTCA CCAGAATGAG GAAGCCGGGA TAGTATAGTT GTGTGAATTC 1140 CAAACTGTCC TGAGGTGCCC CGGAGTGCCA CAGCAAAGTC ACAAGGCTGG CATGGGATAT 1200 TTTAAAACTT TGAGGAAACA CAGAGAGACA TCTGTCAGGC ACCACTTAAC CATCACTACT 1260 AAGTTGTTGG GACCTAACTA CTCAGTAAAT 1290
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