Tag | Content |
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EnhancerAtlas ID | HS190-03266 |
Organism | Homo sapiens |
Tissue/cell | Treg_cell |
Coordinate | chr12:121340420-121341640 |
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 | GTGGCAAACC GGACCTCCGA AATAGGTCTT CCAACTCCAC ACGGCATGCT CGTCCCATTC 60 TATTATGCTC TTTTCTAAGA AGGGAATGTC TACAGTTCTG TCCCAAACCA CATTTGCTTC 120 AAGAGTAAAC CATCTTCAAA CCATTTCTCT AAATTGCAAT CAGGTCCCCC ACTCCTACGA 180 TCATGCCATT TCTTGCTTCC TCACTCTCCA GCTATGACTT CCTTCTCACT ACCCGATTTC 240 CACTCTTCAT GGATACTGCC ATCATTCCTT CAACCCGTCC TGCAAATATC CCACCTCTAC 300 ATGCTAAAGG GAGACCCCTC ATGTTCCTTC CCCCAAACCC TGGCACTCCC TTCTCCGGAT 360 ATGTAGGTTG TCACCCCATA AACTACACAG TAGCTTCTCG CTTCTCGGCC CTTAACGAGC 420 TACTTACTAA CTTTAAAAGC CCCACAGAAA TGAACTTAAC TTGCAGGTCC TCCACCTCCA 480 CACTTGGCCC TGGGCGCCAT TCCTCTGAAA ATAATAGTAC CAACCCTTAC AAAGACTCTG 540 CCCATGCCCC ACTGTCACCA ACGAATTCCT TTTCCAGAAG GAAAAGGAAA CAGGTTCTTC 600 AGGCTCCTCT TCCAACCTCT TCACCAGTGA CTCCCCTCCA AGGTTCGTGG ACTCTACCCC 660 CGCAGTTTTC CTCCCCTCAC TCCCGGGCCT CTGCCCACCT CACCAACTCT CCCTGCGCTC 720 CCTGTCCCAG AGCCAAGCGG CGGCCGCTCC ACTCTCCCAA CTTAGAAGTT CTGCCTCTAT 780 CACCTGTTCT CACTAGAGCT TCCTCTCAGC CCAGCGGCCC ACCTTTGCCC TGGCCTGCCT 840 CTCTCCACCC CTTCGAGTCC TCCTGCCCAG GAAACACCCC CACGAGTCAG TTCCGGGGTG 900 CCTGTCGGAT TCAACTTCCC ATCCGTGGGA TTCCCACCCC CGGGGTCATG CTCCCCTTCT 960 CCATCACCTG CTCCGCCCAT AGCCAGATGA CATCCGCCGC TGCCTCCTCC TCCATTCCCC 1020 TTCTCGGACG CCAGGTCCCC GGCCACTCAC CGCCCTCCGT GCGCGCCAGC CGCCCCCTCC 1080 GGTGGGGAAG AGGGGGGCGT GCACCCCAAC CCGCGCCCCC CCCCCACGAC ACGCACCTGT 1140 TCTTCCTCCT CTTCCCCTCG GCGGGCCGCG CCGGCGCCCC GACCCCCACC CTTGCCGCCT 1200 CCCGGCCTCC CGGAGCCCCG 1220
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