Tag | Content |
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EnhancerAtlas ID | HS062-02775 |
Organism | Homo sapiens |
Tissue/cell | GM18486 |
Coordinate | chr11:44637920-44639030 |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
CTCF | MA0139.1 | chr11:44638591-44638610 | GCACGCCCCCTGCTGGCCA | - | 6.38 | Nr2f6(var.2) | MA0728.1 | chr11:44638892-44638907 | GAGGTCAGGAGGTCA | + | 7.19 | RARA | MA0729.1 | chr11:44638892-44638910 | GAGGTCAGGAGGTCAAGA | + | 6.22 | Zfx | MA0146.2 | chr11:44638868-44638882 | GAGGCCGAGGCGGG | - | 6.01 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_05079 | chr11:44635217-44638910 | Brain_Cingulate_Gyrus | SE_05928 | chr11:44629002-44639061 | Brain_Hippocampus_Middle | SE_08038 | chr11:44634223-44638904 | Brain_Inferior_Temporal_Lobe | SE_10302 | chr11:44637610-44638386 | CD19_Primary | SE_10955 | chr11:44611920-44639025 | CD20 | SE_58811 | chr11:44616581-44638693 | Ly1 | SE_58928 | chr11:44615700-44638774 | Ly3 | SE_65536 | chr11:44638231-44638863 | Pancreatic_islets |
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| Number: 2 | ID | Chromosome | Start | End |
GH11I044616 | chr11 | 44637611 | 44638386 | GH11I044617 | chr11 | 44638481 | 44638710 |
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Enhancer Sequence | TGACCCACAA TTGCTGAGAC TTTGCTAATT TTAGCAAAGT CTGGATGTCA CCAGTGACAT 60 AAACCAGTGC CACCTGACAA GGGACCTGGG AGGAGAAGTG GGTCCCTTGG GAGGTGGTAA 120 GCATCCTACC CTGGAAAGTC ATTGGCTGGT TCTAGATGAT TCTGATGCTG TCAGATGCTG 180 CTTAGGCCGG TGGTAAGTCA GACTCCCAAG GCCTGGAGTG CTAACACTGC CACAGCCGCT 240 AGACCTTTGC TGAGCCTGCT TCCTCATCTA TACAATGGGG CTACTGACCC ATGCCGTGTG 300 AGATACATTG TTAAAGCCTG AAGCACTTAG GCAGCATTTA TTATGTGGTA TGTTGGTGGT 360 GATGTTTTAG TCACCATGCA CATCCATGGA GACACAGGCG GAGGTGGCGT GTGCTGCTGG 420 GGACCAGGTA CAGCCGGAGT CAGGCCAAGG GGTTGCTTGG AAGGAGGCTC TGTCGTAGAC 480 GGGCCAAGGA GACCTGCCTC ATTTTGCTCT GGTGTAGGAT GGCCTGTGGG TGCCCCCAGC 540 CTTGCAGACC TGTGCACCCC TCAGAGGTGC CAGCCTTTTC TTGGAGAGAG GAGGCAGCCC 600 GGCTGCTGGA ACAAGCACCT GTAAACCTGG ATTAGAAACT GCCTGGAGCT GAGCATTTCT 660 GAGTGTGCCT GGCACGCCCC CTGCTGGCCA CTGGCTACTG GTCAGGCGAC ACCCCTCGGA 720 GCTAGGAAGG AAGCGGTCCA GGAACTGACC CCTGCTGTGA CCGTGGCTAT CCCATTGAAT 780 CCTCCCAGGA ACCCCCAGCA TTGCGGGGAT TCACACACAG AGACCTCCTT TAGCACACAG 840 AGCCCGGAAA GGCTTTCTTC TCTCTAGAAC TAGAGCATTT TCTCCTTTAA AATGGCAGAA 900 TTGACCAGCT AGCCAAGGTG GCTCACACCT GTAATCCCAG CACTTTGGGA GGCCGAGGCG 960 GGCGGATCAC TTGAGGTCAG GAGGTCAAGA CCAGCCTGGC CAACATGGTG AAACCCCGTC 1020 TCTACTAAAA ATACAAACAT TAGCCGGGCG TGATGGCGAG TGCCTGTAAT CCCAGCTACT 1080 CAGGAGGCTG AAGCAGGAGA ATCGTTTGAA 1110
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