Tag | Content |
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EnhancerAtlas ID | HS060-08831 |
Organism | Homo sapiens |
Tissue/cell | GM12891 |
Coordinate | chr12:121340410-121341640 |
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) |
ZNF740 | MA0753.2 | chr12:121341532-121341545 | GCGCCCCCCCCCC | + | 6.1 | ZNF740 | MA0753.2 | chr12:121341534-121341547 | GCCCCCCCCCCAC | + | 6.29 |
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| Number of super-enhancer constituents: 1 | ID | Coordinate | Tissue/cell |
SE_27043 | chr12:121340195-121348599 | Esophagus |
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Enhancer Sequence | AAGCAAGTTG GTGGCAAACC GGACCTCCGA AATAGGTCTT CCAACTCCAC ACGGCATGCT 60 CGTCCCATTC TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA 120 CATTTGCTTC AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC 180 ACTCCTACGA TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT 240 ACCCGATTTC CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC 300 CCACCTCTAC ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC 360 TTCTCCGGAT ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC 420 CTTAACGAGC TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC 480 TCCACCTCCA CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC 540 AAAGACTCTG CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA 600 CAGGTTCTTC AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG 660 ACTCTACCCC CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT 720 CCCTGCGCTC CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT 780 CTGCCTCTAT CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC 840 TGGCCTGCCT CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG 900 TTCCGGGGTG CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG 960 CTCCCCTTCT CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC 1020 TCCATTCCCC TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC 1080 CGCCCCCTCC GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC 1140 ACGCACCTGT TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC 1200 CTTGCCGCCT CCCGGCCTCC CGGAGCCCCG 1230
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