Tag | Content |
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EnhancerAtlas ID | HS098-31456 |
Organism | Homo sapiens |
Tissue/cell | HSMM |
Coordinate | chr2:129049810-129051590 |
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) |
CTCF | MA0139.1 | chr2:129050998-129051017 | TGCCACCACCTGCTGGGCA | - | 6.08 | PLAG1 | MA0163.1 | chr2:129051240-129051254 | GGGGCCCACGGGGA | + | 6.72 | STAT1 | MA0137.3 | chr2:129051048-129051059 | TTTCCCAGAAA | - | 6.02 | STAT3 | MA0144.2 | chr2:129050067-129050078 | CTTCCCAGAAG | - | 6.14 | STAT3 | MA0144.2 | chr2:129051048-129051059 | TTTCCCAGAAA | - | 6.32 |
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| Number of super-enhancer constituents: 7 | ID | Coordinate | Tissue/cell |
SE_00963 | chr2:129048730-129053057 | Adrenal_Gland | SE_06274 | chr2:129048977-129053206 | Brain_Hippocampus_Middle | SE_27025 | chr2:129048729-129051744 | Esophagus | SE_41772 | chr2:129050549-129051025 | LNCaP | SE_53946 | chr2:129049968-129051075 | Spleen | SE_65419 | chr2:129048621-129053098 | Pancreatic_islets | SE_68818 | chr2:129048699-129051899 | H9 |
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| Number: 1 | ID | Chromosome | Start | End |
GH02I128290 | chr2 | 129047940 | 129051408 |
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Enhancer Sequence | TGCCAGGCAG TCTGGGCCTG CTCACACCAT GTGTATCCTT CCATAGGGCC CACGCCTGGC 60 AGGACCCTGG CTTGGAGCGG CTTTAACTGT GGCTGGGCTC CTGAGGAGGT AAGGTGGGCC 120 CTGTGTTCCA CGCCCAGCTA CCCACCCAAC ACCTTCTCAG GGCAGGGACG CCCACACCAG 180 TCTGGACACA GAACAACCCG GGGCGAGACA CGTACTGGAG AAGACTGTGC TCCTCACCCC 240 GGCGCTCTGG GACCTTGCTT CCCAGAAGCT GGAAGGAACC AGCCAGGCAT CCCGGCGAGG 300 ATGTGGAGGG TGGTGGTGGG CCCACCCCTG CCTCAGGGAG GGCGGCCAGG CTCACGGGGA 360 GGCTGTGGCA TGTGGGCATG TGAGTGGGCA GGGACAGCCC AGCAAGGGCT GTGGGAAGCC 420 GGGAGGGCAG TGCCCTGTGC AGTGGCTCCA GATTCAGGGC ATTCAGTGTG CAGCAGGCCA 480 GGGCAAATGG CACGGGGGGA ATGGGGCGGA GGGGAGGGGC GGTGACTCAC AAGGCCATGG 540 GGGCGGGCAG AGGAACAAGG GCAGCAGGAA GGGCAGGCAG GGGTGCTATC AGCTGACGGG 600 CTCCTGCTGG AAAAGACGGC TCGACTCACA GGAGGGCACC TGAGACATGG GGTGTGGGGG 660 AAGGCAGCGG TCGGGGAGAG CCTAGGCAGG CCTCCCACTT GTCAGCCTCC CCAACTCTGT 720 TGCCACTCCT ACTGCAAAAG AGCCCTGGAG ACCACCCTGG GTCTGGGGTC CTTGCCGTGG 780 CTGCAGCCCC CCGCTGCCCA CAGCCTGTGT GGTTCCACCC ATGGGCCTGG TGGAGCTGGT 840 CCCTGCTCTG CTCCGCCACA CCAGGCCTCC CTCCCCAAAG GCTGGGCCTT GCTCTGCATG 900 CAGTGGGGCC CAAACCAGCC AGGCACTCCA GCGTCCCACC CGCACACCCT GTCTCCTGCG 960 GAAGGGCACC GCTCCCAGGC ACAGCCCGCT CTGAGCCAGG GGCATGTCAC ACAATATGGC 1020 GCTTTTCTCC TCTTCTGGCC TGGCTCCCCA TAAGCCTGCC CAAGGGCCAG CCTGGGCCTG 1080 GGCAGAGCAA GGCCTGGGAA TGGCTAAGGC TTTGAGGCCT GGAATGAAGC ATGACCGTCA 1140 CTCCCTAAAG CCATGAGTAA AGCTAGTCTG AGGAGTAACT GTGGCGGCTG CCACCACCTG 1200 CTGGGCACTT TCCTTGCAAA CACTGGGGTG GCTCCAGATT TCCCAGAAAC CACTGTTCCT 1260 CATACCCCAG GACGGGAGGG GACCTTCGAA GTTGGAAGGA GAGCAGCAGC AGACCATGGT 1320 CCGAGGGGCG CTTCCCGGGG CCACAGCTTT GGGGGATGTT TAGCAAAACC AGGGGCTGGT 1380 ATGGCCTGGA GGGCCCGGAG TCAGAGGAGG AACATGCTCC CAGATTCTTT GGGGCCCACG 1440 GGGACAGAGG GCAAAGAGAG ACCATCAGGT GGCCTCAGGT CACCAGTGAA GGAAGGCGAG 1500 TTACATTTAT ACCAAGCACC TGTTTTGGGG GTCCTCTGGG GGATGAGGAA GGTTGGATTA 1560 ACCACCAGCT CAGAAGGCCA GTGCTATGTG AGCAGGGTCT GTGGCCACAT AGGATCCAGT 1620 TAGTCCTGTG GTCAGCCTCT AAGTGTGGAA TGGCCATGCT GAGCCAGGCA GAAGCTGACC 1680 CAGTCCTGCT GAACATCCCA GGGCAATGGT TTCACCACAG GTTGGGGGTC CATGCTGAGA 1740 CCACGCTGCA GGGACACAGG GGCACCATGT GGGTCCCGAA 1780
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