Tag | Content |
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EnhancerAtlas ID | HS127-31178 |
Organism | Homo sapiens |
Tissue/cell | Macrophage |
Coordinate | chr8:141059510-141061400 |
SNPs | Number: 3 | ID | Chromosome | Position | Genome Version |
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TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
FOS | MA0476.1 | chr8:141060836-141060847 | AATGAGTCACC | - | 6.02 | JUN(var.2) | MA0489.1 | chr8:141061200-141061214 | AAGGAATGAGTCAT | + | 6.8 | PPARG | MA0066.1 | chr8:141059756-141059776 | GAAGGTCACAGGGACCCCCT | + | 6.8 | ZNF263 | MA0528.1 | chr8:141060812-141060833 | TGGGGAGGGAAGAAGGGGGGA | + | 6.2 |
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| Number: 3 | ID | Chromosome | Start | End |
GH08I140045 | chr8 | 141056052 | 141059854 | GH08I140050 | chr8 | 141060099 | 141060299 | GH08I140051 | chr8 | 141061358 | 141062604 |
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Enhancer Sequence | TATTGTACCC GGGCTCCTGT TCCTTCACTA GGGACCTGCG GAAGGCACAC TGTGGACACT 60 GCGGGAAGAG CCGGCCCTCG GTGATGTGTT CTGCCCACCT CTCATCAAGC ATGAAGATAA 120 ATCCTACAGG GCTCCCCCCC CCGAGACCAC CAAATTATTT CCCTGGCAAC CAGGGAAGTG 180 AATAGAAGGT TATGTATCCC TCCCATTTGC TCGTCGGTCT TTGAAACTCA TATACAGCTG 240 AAAGGGGAAG GTCACAGGGA CCCCCTGTCC AAACACCAAA CCCTGGGATT TCCTTGAGGC 300 TGGAAATGAA AGCGGATCTC TGAGCAGCCT TCCTGAGCGT CTGTATCCCA CAGGGCAGGC 360 ACTGTGTGAG GTTTTGTGGA AGGTCTCCCG CCGAGTCCTC AAGATCATTC TGTGAGGTGC 420 GAGCTTTATT CCTCATTGTA GGGATCAGAA AACTTGTCCA AGATCAAGTG GGAAAGGCTC 480 CTTCAATTCC ACCACAACTC AGTCCCCAAA CTGGATGGCC ATTGAGCAGA TAGTGTGTAA 540 CTGTTGCCTA CACGCCAAAT GACACATGCA GGTGTGAGCG GTGACTGTCA GGCAGGCCAC 600 TGGGGTGTGT AACACCAGGG GCATGAGTAC AGCGTGGGGG CAACAGGGCT AAGCCACTGA 660 GTGTACAAGG GACACCTGGG GACCCATGTT GATAGTGGGG CCACCAGATC TGAGGTCAGC 720 CATGAGCTAG CGAGAGGATT CGGCAATGGA GGCCTTTGGT TTTCACACTG GGCAGCTCAG 780 GCGTAAAGCC TCCAGTGCTT CATGAGTCAT CAAAGCCAAT GAAGAAGTCC TTGGCAGAGG 840 ATTCATTTGA ACTTCCCTTT AACACTTCAG CTGTGGGGAG TCTGGCATGA AATATGCGCA 900 TTAGCTACTC TCCAACTGGA GAATGCAGAA TTAACGTCTG TGGAAAACCT ACATGCTGAG 960 CGATGTGCAC ACACCATCTC ATGCGGTTCT CACAACAATT TCCCACTTTG CAAATCAGGG 1020 GACTGAAGCT CAGAGAAGTA TCATGTTGTG CCTCTACCAG GTGAGATGCC CAACCCCAAC 1080 TCCCACCCCA GGTCCTCCCT CAGTGCCCCC ACCCCATAAA CAGAATTCCC TCTGACACTG 1140 CATGCACCAG CCTCCATGAC TCTCTGGGTC TCATGGTCCC CTGACGGAGG CACACGGGAC 1200 TCAGGACACC CTTCCTCATC CCCAGCACCT CCACCCGGGG CACAGGAAAT GCTCATGAAA 1260 TGTCTATGGA GGAAGAGAGA TGGGAGATGG AGAGATGGGG GCTGGGGAGG GAAGAAGGGG 1320 GGAAGTAATG AGTCACCAGC CTGGGGTCCC ACCTGGAAAC ACCAGATGGG AACAACCCAC 1380 CGACAACCCC AGGAGGGAAA CAATGGCATC CAGCTTCCAG GGCACACACA CTGGGGGGCC 1440 ACACAGCCCT GCACAGGGGG AAGGGCACCT GCACGTGGCC TTCTTTCTCA GCTGGGCATC 1500 TTGGCACTCT CAGGTTCTTC TGGACATTGT CTTCCACGCT GAAGGAACGG AAGTCACCGA 1560 AACAGTCCTT GATGGCTATT TTAGACCTTC AACTGCCATT AAGACACAAT CTCGTACAGA 1620 GAGGGTTTGT GGCCATTCCG TACAAGGAAT TAACAAGTAT GATGAGCTCC CACTACAGAT 1680 AGCATCCTTA AAGGAATGAG TCATCAGAGA CCACCAGATG TTAGCAAGAG AGAAGTGCCT 1740 TCATTCCTGC ACACTCCTCC CTCCCTCATG CCCATTAGAA GACCTGAAGG GGCGGTGGAG 1800 CCTTTAAAAT CAGGGCCACA GGGCCAATGA GACCTCCTCC ATGAGCACCA TGACCTCAGT 1860 GAGCACTGTG GGACCTGCCA GGATGGACAG 1890
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