Tag | Content |
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EnhancerAtlas ID | HS105-18973 |
Organism | Homo sapiens |
Tissue/cell | IMR90 |
Coordinate | chr12:57610810-57611840 |
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) |
KLF16 | MA0741.1 | chr12:57610894-57610905 | GCCCCGCCCCC | + | 6.02 | KLF5 | MA0599.1 | chr12:57610894-57610904 | GCCCCGCCCC | + | 6.02 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_58326 | chr12:57603576-57638314 | Ly1 |
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| Number: 3 | ID | Chromosome | Start | End |
GH12I057218 | chr12 | 57611081 | 57611210 | GH12I057217 | chr12 | 57611281 | 57611390 | GH12I057220 | chr12 | 57611421 | 57611430 |
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Enhancer Sequence | TAAGAGTGGC AGGGCTGGGG CGCTAGCGCG GGCGCGGGGT TCCGGGACGC GAAGGTCCCA 60 GTGTGCGAGG GGCTCCGTGC GCCCGCCCCG CCCCCAGCTC CGAGCGTCCC AACTTTGCGC 120 GGCGCGGGGG AAGCGGACAG ACAGACTGCC CGATTCAGGA CGGGCACTCT CCTAGCGCAA 180 GTTGGCTGAG GCTTGGAGAG GGTGCCGGGC GGAGGTCCCC CTTGCAGCCG ACTTCAGGCG 240 CGGCGGGGGA GGGGACGAAG CCCGACCCGC GAGTGCGCCA GACAGAGCGG GAGTGCGAGA 300 CAGACAGACA AGCCAGCAGG GTGTCAGCCT TGCCGTCTTT CCGCGCCAGT CTCGCTCGCC 360 TGCCTCACTG TCTGTCTGTC CTTCCACCCC TCCACCCCCG CCTTCCCATT TCTCTTCTCT 420 GCACTTGTCA CCATGCCAGG TGGGCTCTGT GTCGGGAGCA TCCATGGCCC GAGCACACAC 480 GCACACACGG ACTCAGGCAG ACACGGCTGA ACTTGGCTAC AGCCAGCCTC CCATCACATT 540 TCCCACGGAG ACACCATCTC CCCTGCACGA CCTCACAGAC ACACCCCCCT CTCGTGCCCC 600 ACTGAAGGGG GAGGCTGTCT GGAAGGGGAG TCTCTCCTCC CATGCCCTCC CTGCCTCCAA 660 CCCCACTCCA AGGCCTCTTT CCCTGAGGCT CTCGGGCGAA GAGCCAGAGG CTAAGGGAGC 720 TCAGACTTGA TCTGCCTCCT TCCTGACTTG GAGGCTTCAA CCTGCGAACA TGCTGTGCTC 780 ATATGTGCTG GGTGGAGGGC GTGGGTCACC GTGTGCACCT GTGTGCATGT GTCCAGGGAA 840 GCCAGGCTTG GTCCAGTACT GGGGCCGAGG GTACATGTGT ATACTGGTGT GGTGTGTGGT 900 GTTGGCTTTG CATGAGTGAG TGTCAGTGCC TGCCTCACAG TGCAGCCATC TGCCTATGCC 960 CCTGGTGTGT GCCCGCAATG GGGGCCCAGG CCCCAGTCCC CCATTTTCCT TCTACCAGCC 1020 TCCCCTGCCT 1030
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